
- •Фогель ф., Мотульски а. Генетика человека: в 3-х т. Т. 3: Пер. С англ. – м.: Мир, 1990. – 366 с.
- •Издательство «мир»
- •7. Эволюция человека
- •7.1. Данные палеоантропологии
- •7.2. Генетические механизмы эволюция видов человека
- •7.2.1. Хромосомная эволюция и видообразование
- •10 7. Эволюция человека
- •7. Эволюция человека 13
- •7. Эволюция человека 15
- •7.2.2. Сравнение сателлитиых днк разных видов высших приматов
- •7. Эволюция человека 17
- •7.2.3 Эволюция белков [1988]
- •18 7. Эволюция человека
- •7 Эволюция человека 19
- •7. Эволюция человека 21
- •22 7. Эволюция человека
- •7. Эволюция человека 23
- •7. Эволюция человека 27
- •7.2.4. Полиморфизм длины рестрикционных фрагментов и эволюция
- •7.2.5. Поведение
- •7.2.6. Изучение ныне существующих первобытных популяций
- •7. Эволюция человека 35
- •7.3. Генетические различия между группами современных людей
- •7.3.1. Расы
- •36 7. Эволюция человека
- •7. Эволюция человека 39
- •40 7. Эволюция человека
- •42 7. Эволюция человека
- •7.3.2. Будущее рас человека: смешение рас
- •8. Генетика и поведение человека
- •8.1. Моделирование на животных
- •8. Генетика и поведение человека 49
- •8.1.1. Исследования на насекомых
- •8. Генетика и поведение человека 53
- •8.1.2. Эксперименты по генетике поведения мышей
- •8. Генетика и поведение человека 55
- •8.2. Генетика поведения человека
- •8. Генетика и поведение человека 61
- •8.2.1. Исследования с помощью классических феиомеиологических методов
- •8.2.1.1. Переоценка классических методов (см. Также гл. 3)
- •8.2.1.2. Задержка умственного развития и умственная отсталость
- •8. Генетика и поведение человека 65
- •8. Генетика и поведение человека 69
- •8.2.1.3. Интеллектуальная деятельность на нормальном и высшем уровнях
- •72 8. Генетика и поведение человека
- •74 8. Генетика и поведение человека
- •8. Генетика и поведение человека 75
- •76 8. Генетика и поведение человека
- •8. Генетика и поведение человека 77
- •78 8. Генетика и поведение человека
- •8. Генетика и поведение человека 81
- •82 8. Генетика и поведение человека
- •8.2.1.4. Специальные познавательные способности и личность
- •8. Генетика и поведение человека 83
- •8.2.1.5. «Аномальное» и социально девиантное поведение
- •90 8. Генетика и поведение человека
- •8.2.2. Хромосомные аберрации и психические расстройства
- •8. Генетика и поведение человека 91
- •8.2.2.1. Аутосомные аберрации
- •8.2.2.2. Аберрации х-хромосомы
- •5.2.2.3. Синдром χύυ
- •100 8. Генетика и поведение человека
- •8. Генетика и поведение человека 101
- •8. Генетика и поведение человека 103
- •8.2.3. Новые подходы, предложенные для исследования генетики поведения человека
- •8.2.3.1. Генетическая изменчивость, которая может влиять на поведение человека
- •8.2.3.2. Генетическая изменчивость вне мозга, влияющая на поведение человека
- •8.2.3.3. Действие гормонов
- •8.2.3.4. Физиология мозга: генетика ээг
- •8.2.3.5. Генетика алкоголизма
- •8.2.3.6. Физиология мозга: генетическая изменчивость нейромедиаторов
- •8. Генетика и поведение человека 121
- •8.2.3.7. Аффективные расстройства и шизофрения
- •8 Генетика и поведение человека 125
- •8. Генетика и поведение человека 135
- •8.2.4. Различия в iq и достижениях между этническими группами
- •136 8. Генетика и поведение человека
- •8. Генетика и поведение человека 141
- •9. Практические аспекты генетики человека и биологическое будущее человечества
- •9.1. Применения генетики человека
- •9.1.1. Генетическое консультирование [71; 90; 101; 129; 136; 149; 205; 2258; 2293; 2323а; 2351]
- •9 Практические аспекты генетики человека 143
- •9. Практические аспекты генетики человека 153
- •9.1,2. Генетический скрининг [2256; 2344; 2350]
- •9. Практические аспекты генетики человека 163
- •9.2. Манипуляции генами
- •9. Практические аспекты генетики человека 165
- •9. Практические аспекты генетики человека 169
- •9. Практические аспекты генетики человека 173
- •9.3. Биологическое будущее человечества
- •9. Практические аспекты генетики человека 175
- •9. Практические аспекты генетики человека 177
- •Приложение 1 Методы подсчета генных частот
- •182 Приложение 1
- •184 Приложение 1
- •Приложение 2 Анализ сегрегации распространенных признаков: отсутствие смещений вследствие регистрации, доминирование [876; 877]
- •Приложение 3 Формулы и таблицы для коррекции регистрационных смещений, а также для тестирования и оценки сегрегационных отношений. Другие статистические проблемы и вычислительный пример
- •192 Приложение 3
- •194 Приложение 3
- •Приложение 4 Мультифакториальное наследование и главные гены
- •204 Приложение 4
- •206 Приложение 4
- •208 Приложение 4
- •Приложение 5 Диагностика зиготности
- •Приложение 6 Вычисление коэффициента наследуемости по близнецовым данным
- •224 Приложение 6
- •Приложение 7 Метод путевых коэффициентов
- •230 Приложение 7
- •Приложение 8 Медико-генетическое консультирование: использование условных вероятностей
- •234 Приложение 8
- •236 Приложение 8
- •240 Приложение 8
- •Приложение 9 Примеры расчета сцепления
- •Литература
- •252 Литература
- •Литература к введению и главе 1
- •Литература к главе 2
- •256 Литература
- •258 Литература
- •260 Литература
- •262 Литература
- •Литература к главе 3 и к приложениям 1, 2, 3, 4, 5, 6, 7, 9
- •266 Литература
- •270 Литература
- •Литература к главе 4
- •278 Литература
- •282 Литература
- •284 Литература
- •286 Литература
- •288 Литература
- •Литература к главе 5
- •290 Литература
- •Литература к главе 6
- •300 Литература
- •302 Литература
- •304 Литература
- •Литература к главе 7
- •306 Литература
- •Литература к главе 8
- •308 Литература
- •310 Литература
- •Литература к главе 9 и приложению 8
- •Предметный указатель1)
- •324 Предметный указатель
- •344 Предметный указатель
- •356 Предметный указатель
- •364 Предметный указатель
- •Оглавление
- •7. Эволюция человека 5
- •8. Генетика и поведение человека . . 47
- •9. Практические аспекты генетики человека и биологическое будущее человечества 142
- •Электронное оглавление
- •7. Эволюция человека 5
- •8. Генетика и поведение человека 63
- •9. Практические аспекты генетики человека и биологическое будущее человечества 213
- •Назад к электронному оглавлению
290 Литература
Danieli G. Α., Mostacciuolo M.L., Pilotto G., Angelini С., Bonfante A. (1980). Duchenne muscular dystrophy. Data from family studies, Hum. Genet, 54, 63-68.
Davie A.M., Emery A.E.H. (1978). Estimation of proportion of new mutants among cases of Duchenne muscular dystrophy, J. Med. Genet., 15, 339-345.
Davies K. E., Harper K., Bonthron D., Krumlauf R., Polkey Α., Pembrey M.W., Williamson R. (1984). Use of a chromosome 21 cloned DNA probe for the analysis of nondisjunction in Down Syndrome, Hum. Genet, 66, 54-56.
DeGroot L.J., Paloyan E. (1973). Thyroid carcinoma and radiation. A Chicago endemic, J. Am. Med. Assoc., 225, 487-491.
Demerec M. (1937). Frequency of spontaneous mutations in certain stocks of Drosophila melanogaster, Genetics, 22, 469.
Deng Shaozhuang et al. (1982). Birth survey in high background radiation area, Chin. J. Radiol. Med. Protection, 2, 60.
DeuelT.F., Huang J. S. (1984). Roles of growth factor activities in oncogenesis, Blood, 64, 951-958.
Dhadial R.K Machim A.M., Tait S.M. (1970). Chromosomal anomalies in spontaneously aborted human fetuses, Lancet, II, 20-21.
Drake J. W. (ed.) (1973). Proceedings of an International Workshop on the Genetic Control of Mutation, Genetics [Suppl.], 73.
l439a.Duckworth-Rysiecki G., Cornish K., Clarke C.A., Buchwald M. (1985). Identification of two complementation groups in Fanconi anemia, Somatic Cell and Mol. Genet, 11, 35-41.
Ehling U.H. (1982). Risk estimate based on germ cell mutations in mice. In: Sugimura T., Kondo S., Takebe H. (eds.), Environmental mutagens and carcinogens, Proc. 3rd Intern. Conf. on Environmental Mutagens, Univ. of Tokyo Press. Tokyo and A. Liss, New York, pp. 709-719.
Ek J. (1959). Thyroid function in mothers of mongoloid infants, Acta Paediatr., 48, 33-42.
Epstein C. J., Martin G. M., Schultz A. L., Motulsky A. G. (1966). Werner's syndrome: A review of its symptomatology. Natural history, pathological features, genetics and relationship to the natural aging process, Medicine, 45, 177-221.
Erickson J.D. (1979). Paternal age and Down syndrome, Amer. J. Hum. Genet, 31, 489-497.
Erickson J.D., Bjerkedal T. (1981). Down syndrome associated with father's age in Norway, J. of Med. Genet, 18, 22 -28.
Evans J. A., Hunter A. G. W., Hamerton J. L. (1978). Down syndrome and recent geographic trends in Manitoba, J. Med. Genet, 15, 4347.
Ferguson-Smith Μ.Α., Handmaker S.D. (1961). Observations on the satellited human chromosomes, Lancet, I, 638-640.
Fialkow P.J. (1967). Autoantibodies and chromosomal aberration, Lancet, I, 1106.
Fialkow P.J. (1967). Thyroid antibodies,
Down's syndrome and maternal age, Nature, 214, 1253-1254.
Fialkow P.J. (1977). Clonal origin and stem cell evolution of human tumors. In: Genetics of Human Cancer, Mulvihill J. J., Miller R. W., Fraumeni J. F. Jr (eds.), Raven, New York, pp. 439-453.
Fischer E., Thielmann H. W., Neundörfer В., Rentsch F.J., Edler L., Jung E.G. (1982). Xeroderma pigmentosum patients from Germany: Clinical symptoms and DNA repair characteristics, Arch. Dermatol. Res., 274, 229-247.
Fitzgerald P. H., Stewart J., Suckling R. D. (1983). Retinoblastoma mutation rate in New Zealand and support for the two-hit model, Hum. Genet, 64, 128-130.
Ford C.E. (1970). Cytogenetics and sex determination in man and mammals, J. Biosoc. Sei. [Suppl.], 2, 7-30.
FordC.E., Evans E. P., Searle A.G. (1978). Failure of irradiation to induce Robertsonian translocations in germ cells of male mice. In: Conference on Mutations: Their origin, nature and potential relevance to genetic risk in man, Jahreskonferenz 1977, Zentrallaboratorium für Mutagenitätsprüfungen, H. Boldt Verlag, Boppard, pp. 102-108.
Ford C. E., Searle A. G., Evans E. P., West B. J. (1969). Differential transmission of translocations induced in spermatogonia of mice by X-irradiation, Cytogenetics, 8, 447-470.
Francke U., Benirschke K., Jones O. W. (1975). Prenatal diagnosis of trisomy 9, Hum. Genet, 29, 243-250.
Francke U., Felsenstein J., Gartier S. M., Migeon B. R., Dancis J., Seegmiller J. E., Bakay F., Nyhan W.L. (1976). The occurence of new mutants in the X-linked recessive LeschNyhan disease, Am. J. Hum. Genet, 28, 123-137.
Freese E. (1963). Molecular mechanism of mutations. In: Molecular genetics, Taylor J.H. (ed.), Plenum, New York, pp. 207-269.
Freese E. (1971). Molecular mechanisms of mutations. In: Chemical mutagens, HollaenderA. (ed.), Vol. 1, Plenum, New York, pp. 1-56.
Fulder S.J., Holliday R. (1975). A rapid rise in cell variants during the senescence of populations of human fibroblasts, Cell, 6, 67-73.
Gardner R.J.M. (1977). A new estimate of the achondroplasia mutation rate, Clin. Genet, 11, 31-38.
Gebhardt E. (1974). Antimutagens, Data and problems (review), Hum. Genet., 24, 1-32.
Gebhart E. (1981). Sister chromatid exchange (SCE) and structural chromosome aberration in mutagenicity testing, Hum. Genet., 58, 235-254.
Geissler E., Theile M. (1983). Virus-induced gene mutations of eukaryotic cells, Hum. Genet, 63, 1-12.
German J. (ed.). (1983). Chromosome mutation and neoplasia, AR Liss, New York.
Литература 291
German J. (1983). Neoplasia and chromosome-breakage syndromes. In: Chromosome mutation and neoplasia, German J. (ed.), AR Liss, New York, pp. 97-134.
German J., Bloom D., Archibald R. (1965). Chromosome breakage in a rare and probably genetically determined syndrome of man, Science, 148, 506-507.
Gilbert F. (1983). Retinoblastoma and recessive alleles in tumorigenesis, Nature, 305, 761-762.
Glatt H., Oesch F. (1984). Variations in epoxide hydrolast activities in human liver and blood. In: C. H. S. Banbury Report 16, Genetic Variability in Responses to Chemical Exposure, OmennG.S., GelboinH.V. (eds.), Cold Spring Harbor Laboratory, pp. 189-201.
Gropp A., Platz G. (1967). Chromosome breakage and blastic transformation of lymphocytes in ataxiateleangiectasia, Hum. Genet, 5, 77-79.
Grüneberg H. (1970). Das Problem der Mutationsbelastung. In: Genetic and Geselschaft Wendt G. G. (ed.), Wissenschaftliche Verlagsanstalt, Stuttgart, pp. 72-77.
Günther M., PenroseL.S. (1935). The genetics of epiloia, J. Genet., 34, 413-430.
Haldane J.B.S. (1935). The rate of spontaneous mutation of a human gene, J. Genet., 31, 317-326.
Haldane J. B. S. (1939). The spread of harmful autosomal recessive genes in human populations, Ann. Eugen, 9, 232-237.
Haldane J.B.S. (1947). The mutation rate of the gene for hemophilia, and its segregation ration in males and females, Ann. Eugen, 13, 262-271.
Hansemann D. von (1890). Über asymetrische Zellteilung in Epithelkrebsen und deren biologische Bedeutung, Virchow's Arch. Pathol. Anat, 119, 299-326.
Hansteen l.-L., Varslot K., Steen-Johnsen J., Langard S. (1982). Cytogenetic screening of a newborn population, Clin. Genet., 21, 309-314.
Harnden D. G. (1974). Ataxia teleangiectasia syndrome: Cytogenetic and cancer aspects. In: Chromosomes and cancer, German J. (ed.), Raven, New York, pp. 87-104.
Harnden D.G. (1977). Cytogenetics of human neoplasia. In: Genetics of human cancer, Mulvihill J.J., Miller R.W., FraumeniJ.F. Jr. (eds.), Raven, New York, pp. 87-104.
Harnden D. G. (1974). Viruses, chromosomes, and tumors: The interaction between viruses and chromosomes. In: German J. (ed.), Chromosomes and Cancer, J. Wiley and Sons, New York, pp. 151-190.
Hassold T., Jacobs P., Kline J., Stein Z., Warburton D. (1981). Effect of maternal age on autosomal trisomies, Ann. Hum. Genet, 44, 29-36.
Hassold T.J., Jacobs P.A. (1984). Trisomy in man, Ann. Rev. Genet, 18, 69-77.
Hayes A., Costa T., Scriver C. R., Childs B.
(1985). The effect of Mendelian disease on human health. II. Response to treatment Am. J. Med. Genet, 21, 243-255.
Hayflik L. (1965). The limited in vitro lifetime of diploid cell strains, Exp. Cell. Res., 37, 614-636.
Hayflik L., MoorheadP.S. (1961). The serial cultivation of human diploid cell strains, Exp. Cell Res., 25, 585-621.
Hecht F., Kaiser McCaw B. (1977). Chromosome instability syndromes. In: Genetics of human cancer, Milvihill J. J., Miller R. W., Fraumeni J. F. (eds.), Raven, New York, pp. 105-123.
Herrmann J. (1966). Der Einfluss des Zeugungsalters auf die Mutation zu Hämophilie Α., Hum. Genet, 3, 1-16.
High Background Radiation Research Group, China (1980). Health survey in high background radiation area in China, Science, 209, 877-880.
Hirschhorn K. (1968). Cytogenetic alterations in leukemia. In: Perspectives in leukemia, Dameshek W., Dutcher R. M. (eds.), Grune and Stratton, New York, pp. 113-122.
Hollaender A. (ed.) (1973). Chemical mutagens. Principles and methods for their detection, Plenum, New York, Vol. I/II 1971; Vol. Ill, 1973.
Holliday R., Kirkwood T. B. L. (1981). Predictions of the somatic mutation and mortalisation theories of cellular ageing are contrary to experimental observations, J. Theor. BioL, 93, 627-642.
HookE.B. (1981). Unbalanced Robertsonian translocations associated with Down's syndrome or Patau's syndrome: Chromosome subtype, proportion inherited, mutation rates and sex ratio, Hum. Genet, 59, 235-239.
Hook E. В., Cross P. К. (1981). Temporal increase in the rate of Down syndrome livebriths to older mothers in New York State, J. Med. Genet, 18, 29-30.
HookE.B., Cross P. K. (1982). Paternal age and Down's syndrome genotype diagnosed prenatally: No association in New York State data, Hum. Genet, 62, 167-174.
Hook E. В., Cross P. К., Regal R.R. (1984). The frequency of 47, +21,47, +18 and 47, + 13 at the uppermost extremes of maternal ages: results on 56094 fetuses studied prenatally and comparisons with data on livebirths, Hum. Genet, 68, 211-220.
Hook KB., Regal R.R. (1984). A search for a paternal age-effect upon cases of 47, +21 in which the extra chromosome is of paternal origin, Am. J. Hum. Genet, 36, 413-421.
Hook E.B., Schreinemachers D.M., Wüley A.M., Cross P. K. (1983). Rates of mutant structural chromosome rearrangements in human fetuses: Data from prenatal Cytogenetic studies and associations with maternal age and parental mutagen exposure, Amer. J. Hum. Genet, 35, 96-109.
Ishimaru T., Cihak R. W., Land C.E., Steer A.,
292 Литература
Yamada A. (1975). Lung cancer at autopsy in A-bomb survivors and controls, Hiroshima and Nagasaki, 1961-1970. II. Smoking, occuration and A-bomb exposure, Cancer, 36, 1723-1728.
luchil. (1968). Abnormal hemoglobin in Japan: Biochemical and epidemiolpgic characters of abnormal hemoglobin in Japan, Acta Haematol, Jpn., 31, 842-851.
Jablon S., Kato H. (1970). Childhood cancer in relation to prenatal exposure to A-bomb radiation, Lancet, II, 1000.
Jacobs P.A. (1981). Mutation rates of structural chromosome rearrangements in man, Amer. J. Hum. Genet., 33, 44-45.
Jacobs P. A., Frakiewitz A., Law P. (1972). Incidence and mutation rates of structural rearrangements of the autosomes in man, Ann. Hum. Genet., 35, 301 319.
Jacobs P. A., Funkhauser J., Matsuura J. (1981). In: Hook E.B., Porter I.H. (eds.), Population and biological aspects of human mutation, Academic Press, New York, London, pp. 133-145.
Jacob P.A., Mayer M. (1981). The origin of human trisomy: A study of heteromorphisms and satellite associations, Ann. Hum. Genet., 45, 357-365.
Jacobs P. A., Morton N.E. (1977). Origin of human trisomies and polyploids, Hum. Hered., 27, 59-72.
Janerich D. T., Flink E. M., Keogh M. D. (1976). Down's syndrome and oral contraceptive usage, Br. J. Obstet. Gynaecol., 83, 617-620.
Jones K. L., Smith D. W., Hervey M. A. S., Hall B.D., QuanL. (1975). Older paternal age and fresh gene mutation: Data on additional disorders, J. Pediatr., 86, 84-88.
Jongbloet P.H., Mulder A., Homers A. J. (1982). Seasonality of рге-ovulatory nondisjunction and the aetiology of Down syndrome, A European collaborative study, Hum. Genet., 62, 134-138.
Kemp T. (1940). Altern and Lebensdauer. In: Handbuch der Erbbiologie des Menschen, Just G. (ed.), Springer Verlag, Berlin, pp. 408 421.
KerrC.B. (1965). Genetics of human blood coagulation, J. Med. Genet, 2, 254.
Kimura M. (1968). Evolutionary rate at the molecular level, Nature, 217, 624-626.
Kimura M., Ohta T. (1973). Mutation and evolution at the molecular level, Genetics [Suppl.], 73, 19-35.
King J.L. (1971). The role of mutation in evolution, Proceedings of the 6th Berkeley Symposium on Mathematical Statistics and Probability, University of California Press, Berkeley, pp. 69-100.
KirkwoodT.B.L., Cremer Th. (1982). Cytogerontology since 1881: A reappraisal of August Weisman and a review of modern progress, Hum. Genet, 60, 101-121.
Klamerth O.L. (1976). Inhibition of transcrip-
tion by isonicotinic and hydrazide, Mutât. Res., 35, 53-64.
Klamerth O.L. (1978). Inhibition of post-replication repair by isonicotinic and hydrazide, Mutât Res., 50, 251-261.
Klose J. (1975). Protein mapping by combined isoelectric focusing and electrophoresis of mouse tissue, Hum. Genet, 26, 231-243.
Klose J., Blohm J., Gerner I. (1977). The use of isoelectric focusing and electrophoresis to obtain highly complex-protein patterns of mouse embryos. In: Methods in prenatal toxicology, Neubert D., Merker H.-J., Kwasrigroch T. E. (eds.), Thieme, Stuttgart, pp. 303313.
KnudsonA.G. (1971). Mutation and cancer: Statistical study of retinoblastoma, Proc. Natl. Acad. Sei. USA, 68, 820-823.
KnudsonA.G. (1973). Mutation and human cancer, Adv. Cane. Res., 17, 317-352.
Knudson A. G. (1977). Genetics and etiology of human cancer, Adv. Hum. Genet, 8, 1-66.
Knudson A. G., Hethcote H. W., Brown B. W. (1975). Mutation and childhood cancer. A probabilistic model for the incidence of retinoblastoma, Proc. Natl. Acad. Sei. USA, 72, 5116-5120.
KnudsonA.G., Strong L.C. (1972). Mutation and cancer: Neuroblastoma and pheochromocytoma, Am. J. Hum. Genet, 24, 514-532.
Kochupillai N.. Verma J.C., Grewal M.S., Ramalingaswami V. (1976). Down's syndrome and related abnormalities in an area of high background radiation in coastal Kerala, Nature, 262, 60-61.
Kondo S. (1973). Evidence that mutations are induced by error in repair and replication. In: Workshop on the Genetic Control of Mutation, Genetics [Suppl.], 73, 109-122.
Koufos A., Hansen M. F., Copeland N.G., Jenkins Ν.Α., Lampkin B.C., Cavenee W.K. (1985). Loss of heterozygosity in three embryonal tumours suggests a common pathogenetic mechanism, Nature, 316, 330-334.
Langenbeck 17., Hansmann L, Hinney В., Honig V. (1976). On the origin of the supernumerary chromosome in autosomal trisomieswith special reference to Down's Syndrome, Hum. Genet, 33, 89-102.
Lawry R. В., Jones D. C., Renwick D. H. G., Trimble B.K. (1976). Down syndrome in British Columbia, 1972-1973: Incidence and mean maternal age, Teratology, 14, 29-34.
Lea D.E., Catcheside D.G. (1942). The mechanism of the induction by radiation of chromosomes aberrations in Tradescantia, J. Genet, 44, 216-245.
LeBeau M., 'Rowley J.D. (1984). Heritable fragile sites in cancer, Nature, 308, 607-608.
Lejeune J., Turpin R., Rethoré M.O. (I960). Les enfants nés de parents irradiés (Cas particuliers de la sex-ratio), 9th International Congress Radiology, 23-30.7,1959, München, pp. 1089-1096.
Lele K.P., Penrose L.S., Stallard H.B. (1963).
Литература 293
Chromosome deletion in a case of retinoblastoma, Ann. Hum. Genet, 27, 171.
Lenz W. (1959). Die Abhängigkeit der Missbildungen vom Alter der Eltern, Verh. Dtsch. Ges. Inn. Med., 64, Kongr. Bergmann Verlag, München, pp. 74-88.
Lindgren D. (1972). The temperature influence on the spontaneous mutation rate. I. Literature review, Hereditas, 70, 165-178.
Lindsten J., Marsk L., Berglund K., Iselius L., Ryman N., Annerén G., Kjessler В., Mitelman F., Nordenson L, Wahlström J., Vejlens L. (1981). Incidence of Down's syndrome in Sweden during the years 1968-1977. In: Burgio et al. (eds.), Trisomy 21, Springer, Berlin, Heidelberg, New York, pp. 195-210.
Lu Bingxin et al. (1982). Survey of hereditary ophthalmopathies and congenital ophthalmic malformations in high background areas, Chin. J. Radiol. Med. and Protection, 2, 58-59.
Lüers H. (1955). Zur Frage der Erbschädigung durch tumortherapeutische Cytostatica, Z. Krebsforsch., 60, 528.
Lüning K. G., Searle A. G. (1970). Estimates of the genetic risks from ionising irradiation, Mutation Res., 12, 291-304.
LuriaS.E., Delbrück M. (1943). Mutations of bacteria fron virus sensitivity to virus resistance, Genetics, 28, 491.
Lynas M.A. (1956/57). Dystrophia myotonica with special reference to Northern Ireland, Ann. Hum. Genet, 21, 318-351.
Lynch H. T. (1976). Miscellaneous problems, cancer and genetics. In: Lynch H. T. (ed.), Cancer genetics, Thomas, Springfield.
Lyon M. F., Philipps R. J. S. (1975). Specific locus mutation rates after repeated small radiation doses to mouse oocytes, Mutation Res., 30, 375-382.
Mackenzie H.J., Penrose LS. (1951). Two pedigrees of ectodactyly, Ann. Eugen, 16, 88.
MagenisR.E., OvertonK.N., Chamberlin J., Brady T., Lovrien E. (1977). Parental origin of the extra chromosome in Down's syndrome, Hum. Genet, 37, 7-16.
Mailing H. V., DeSerres F.J. (1973). Genetic alternations at the molecular level in X-ray induced ad-3B mutants of Neurospora crassa, Radiât. Res., 53, 77-87.
Mark J. (1974). Cytogenetics of the human meningioma. In: German J. (ed). Chromosomes and cancer, J. Wiley and Sons, New York, pp. 497-517.
Marsden C.D. (1982). Neurotransmitters and CNS disease: Basal ganglia disease, The Lancet, II, 1141-1146.
Martin C. M., Sprague C. A., Epstein C. J. (1970). Replicative lifespan of cultivated human cells: Effect of donor's age, tissue and genotype, Lab. Invest, 23, 86-92.
Matsunaga E. (1976). Hereditary retinoblastoma: Penetrance, expressivity and age of onset, Hum. Genet, 33, 1-15.
Matsunaga E. (1981). Genetics of Wilm's tumor, Hum. Genet, 57, 231-246.
Matsunaga E., Tonomura A., Oishi H., Kikuchi Y. (1978). Reexamination of paternal age effect in Down's syndrome, Hum. Genet, 40, 259-268.
Mattet J. F., Mattel M. G., Ayme S., Siraud F. (1979). Origin of the extra chromosome in trisomy 21, Hum. Genet. 46, 107-110.
Manor J. W. (1924). The production of nondisjunction by X-rays, J. Exp. Zool., 39, 381-432.
McCannJ., Ames B.N. (1976). Detection of carcinogens as mutagens in the Salmonella/microsome test: Assay of 300 chemicals, Discussion, Proc. Natl. Acad. Sei. USA, 73, 950-954.
McCannJ., Choi E., Yamasaki E., Ames B.N. (1975). Detection of carcinogens as mutagens in the Salmonella/microsome test: Assay of 300 chemicals, Proc. Natl. Acad. Sei. USA, 72, 5133-5139.
McGregor D. H., et al. (1977). Breast cancer incidence among atomic bomb survivors, Hiroshima and Nagasaki, 1950-1969, J. Natl. Cancer Inst, 59, 799-811.
Mikkelsen M., Fischer G., Stene J.,, Petersen E. (1976). Incidence study of Down's syndrome in Copenhagen, 1960-1971: With chromosome investigation, Ann. Hum. Genet, 40, 177-182.
Miller R. W. (1969). Delayed radiation effects in atomic bomb survivors, Science, 166, 569.
Mohn G., Wùrgler F.F. (1972). Mutator genes in different species, Hum. Genet, 16, 49-58.
Money Α., Cox S., Holliday R. (1982). Human lymphocytes resistant to 6-thioguanine resistance increase with age, Mech. Ageing. Dev., 19, 21-26.
Morton N.E., LaloueU.M. (1978). Genetic counseling in sex linkage, Birth Defects Conference, San Francisco, 11-14 June 1978.
Morton N.E., Lindsten J. (1976). Surveillance of Down's syndrome as a paradigm of population monitoring, Hum. Hered., 26, 360-371.
Mjllenbach C.J. (1974). Mediate defekter i ojets indre hinder klinik og arvelighedsforhold, Munksgaard, Kopenhagen.
Motulsky A. G. (1968). Some evolutionary implications of biochemical variants in man, Proceedings of the 8th International Congress of the Anthropology and Ethnology Society, September 1968, Tokyo.
Motulsky A. G. (1982). Interspecies and human genetic variation, problems of risk assessment ih chemical mutagenesis and carcinogenesis. In: Chemical Mutagenesis, Human Population Monitoring and Genetic Risk Assessment (Progress in Mutation Research, Vol. 3), Bora K. C., Douglas G. R., Nestmann E. R. (eds.), Elsevier Biomédical Press, pp. 75-83.
Motulsky A. G. (1984). Environmental mutagenesis and disease in human populations. In: Mutation, Cancer, and Malformation, Chu
294 Литература
E.H.Y. Generoso W. M. (eds.), Plenum, New York, pp. 1-11.
Muller H.J. (1972). Artificial transmutation of the gene, Science, 66, 84-87.
Muller H.J. (1955). Artificial transmutation of genes. In: Great experiments in biology, Gabriel M. L., Fogel S. (eds.), Prentice Hall, Englewood Chiffs (Reprint of the 1927 paper), pp. 260-266.
Mulvihill J. J., Miller R. W., Fraumeni J. F. Jr. (eds.) (1977). Genetics of human cancer, Raven, New York.
Murdoch J. L, Walker Β. Α., Hall J. G., Abbey H., Smith K.K., McKusick V.A. (1970). Achondroplasia-A genetic and statistical survey, Ann. Hum. Genet, 33, 227.
Murdoch J., Walker Β.Α., McKusick V.A. (1972). Parental age effects on the occurence of new mutations for the Marfan syndrome, Ann. Hum. Genet., 35, 331-336.
NeelJ.V. (1957). Some problems in the estimation of spontaneous mutation rates in animals and man: Effects of radiation on human heredity, WHO, Geneva, pp. 139150.
NeelJ.V. (1981). Genetics effects of atomic bombs, Science, 213, 1206.
Neel J. V., Kato H., Schul! W.J. (1974). Mortality in the children of atomic bomb survivors and controls, Genetics, 76, 311-326.
Neel J. V., Mohrenweiser H., Satoh С., Hamilton В. (1979). A consideration of two biochemical approaches to monitoring human populations for a change in germ cell mutation rates. In: Berg K. (ed.), Genetic damage in man caused by environmental agents, Academic Press, New York, etc., pp. 29-47.
NeelJ.V., Mohrenweiser H. W., Meisler M. H. (1980). Rate of spontaneous mutation of human loci encoding protein structure, Proc. Natl. Acad. Sei. USA, 77, 6037-6041.
Neel J. V., Schull W.J. et al. (1956). The effect of exposure to the atomic bombs on pregnancy termination in Hiroshima and Nagasaki, Nat. Acad. Sei. Natl. Res. Counc. Publ., Washington (DC), 461.
Neel J. V., Tiffany Т.О., Anderson N.G. (1973). Approaches to monitoring human populations for mutation rates and genetic disease, Chemical mutagens, Hoelaender A. (ed.), Vol. 3, Plenum, New York, pp. 105-150.
Neel J.V., Veda N., Satoh C., Ferrell R.E., Tonis R.J., Hamilton H.B. (1978). The frequency in Japanese of genetic variants of 22 proteins. V. Summary and comparison with data on Caucasians from the British isles, Ann. Hum. Genet., 41, 429-441.
Newcombe H.B. (1965). The study of mutation and selection in human populations, Eugen. Rev., 57, 109-125.
Newcombe H. В., McGregor F. (1964). Learning ability and physical wellbeing in offspring from rat populations irradiated over many generations, Genetics, 50, 1065-1081.
IS&Qn. Nielsen J. (1966). Diabetes mellitus in pa-
rents of patients with Klinefelters' syndrome, Lancet, I, 1376.
Nielsen J., Sillesen I. (1975). Incidence of chromosome aberration among 11, 148 newborn children, Hum. Genet., 30, 1-12.
Nielsen J., Wohlert M., Faaborg-Andersen J., Hansen К., Hvidman L, Krag-Olsen В., Moulvad I., Videbech P. (1982). Incidence of chromosome abnormalities in newborn children. Comparison between incidences in 1969-1974 and 1980-1982 in the same area, Hum. Genet., 61, 98-101.
Nilsson C., Hansson A., Nilsson G. (1975). Influence of thyroid hormones to satellite association in man and the origin of chromosome abnormalities, Hereditas, 80, 157-166.
Nowell P. C., Hungerford D. A. (1960). A minute chromosome in human chronic granulocytic leukemia, Science, 132, 1497.
Oehlkers F. (1943). Die Auslösung von Chromosomenmutationen in der Meiosis durch Einwirkung von Chemikalien, Z. Induktiven Abstammungs-Vererbungslehre, 81, 313341.
Oehme R., Kahne E., Kleihauer E., Horst J. (1983). HbM Milwaukee: Direct detection of the ß-globin gene mutation of an afflicted family, Hum. Genet., 64, 376-379.
Oertelt R. (1970). Klinisch-genetische Analyse des von Hippel-Lindau-Syndroms: Ausgehend von den Anginoblastomen des Kleinhirns, University of Heidelberg, MD Dissertation.
Ohno S. (1972). Gene duplication, mutation
load, and mammalian genetic regulatory systems, J. Med. Genet., 9, 254.
Pearson M., Rowley J.Z. (1985). The relation of oncogenesis and cytogenetics in leukemia and lymphoma, Ann. Rev. Med., 36, 471-483.
Penrose L.S. (1933). The relative effects of paternal and maternal age in mongolism, J. Genet, 27, 219-224.
1590a. Penrose L.S. (1955). Parental age and mutation, Lancet, П, 312.
1591. Penrose L.S. (1957). Parental age in achondroplasia and mongolism, Am. J. Hum. Genet, 9, 167-169.
I59ln. Pfeiffer R.A. (1964). Dominant erbliche Akrocephalosyndaktylie, Z. Kinderheilkd, 90, 301.
1592. Propping P., Buselmaier W., Röhrborn G. (1973). Kritische Betrachtung über die intraanimale Kultur von Microorganismen, eine Methode zum Nachweis chemisch induzierter Mutationen, Arzneim Forsch., 6, 746-749.
\593.RapoportI.A. (1946). Carbonyl compounds and the chemical mechanism of mutation, CR Acad. Sei. USSR, 54, 65.
RatnoffO.D., Bennett B. (1973). The genetics of hereditary disorders of blood coagulation, Science, 179, 1291-1298.
Reed Т.Е. (1959). The definition of relative fitness of individuals with specific genetic traits, Am. J. Hum. Genet, 11, 137.
Reed Т.Е., Falls H.F. (1955). A pedigree of aniridia with a discussion of germinal mosai-
Литература 295
cism in man, Am. J. Hum. Genet, 7, 28-38.
1597. Reed Т.Е., NeelJ.V. (1955). A genetic study of multiple pplyposis of the colon (with an appendix deriving a method for estimating relative fitness), Am. J. Hum. Genet., 7, 236-263.
\591a. Reichert W., Buselmaier W., Vogel F. (1984). Elimination of X-ray-induced chromosomal aberrations in the progeny of female mice, Mutation Res., 139, 87-94.
Reith W. (1970). Mutationen zu Hämophilie A. Häufigkeit im Regierungsbezirk Münster and Abhängigkeit von Zeugungsalter, University of Münster, MD Dissertation.
Rischbieth H., Barrington A. (1912). Treasury of human inheritance, Parts VII and VIII, Section XV A: Dwarfism, University of London, Dulau London, pp. 355-573.
Röhrborn G. (1965). Über mögliche mutagene Nebenwirkungen von Arzneimitteln beim Menschen, Hum. Genet., I, 205-231.
Röhrborn G., Berrang H. (1967). Dominant lethals in young female mice, Mutât. Res., 4, 231-233.
Röhrborn G. (1970). Biochemical mechanisms of mutation. In: Chemical mutagenesis in mammals and man, Vogel F., Röhrborn G. (eds.), Springer, Berlin, Heidelberg, New York, pp. 1-15.
Röhrborn G. (1970). The dominant lethals: Method and cytogenetic examination of early cleavage stages. In: Chemical mutagenesis in mammals and man, Vogel F., Röhrborn G. (eds.), Springer, Berlin, Heidelberg, New York, pp. 148-155.
Röhrborn G., Buckel U. (1976). Investigation on the frequency of chromosome aberrations in bone marrow cells of Chinese hamsters after simultaneous application of caffeine and cyclophosphamide, Hum. Genet., 33., 113-119.
Röhrborn G. et al. (1978). A correlated study of the cytogenetic effect of INH on cell systems of mammals and man conducted by thirteen laboratories, Hum. Genet., 42, 1-60.
Roth M. P., Feingold J., Baumgarten Α., Bigel P., Stall C. (1983). Reexamination of paternal age effect in Down's syndrome, Hum. Genet., 63, 149-152.
Russell L. B., de Homer D. L, Montgomery С. S. (1973). Analysis of c-locus region by means of complementation testing and biochemical studies, Biol. Div. Ann. Prog. Rep. ORNL-4915, 101-103.
Russell L. B., de Homer D. L., Montgomery С. S. (1974). Analysis of 30 c-locus lethals by variability of biochemical studies, Biol. Div. Ann. Prog. Rep. ORNL-4993, 119-120.
Russell W.L, Kelly E.M., Hunsicker P. R. et al. (1972). Effect of radiation dose-rate on the induction of X-chromosome loss in female mice. In: United Nations, Report of the United Nations Science Committee on the Effect of Atomic Radiations. Ionizing radia-
tion: levels and effects, Vol. II, Effect, New York.
Russell W.L (1965). Effect of the interval between irradiation and conception on mutation frequency in female mice, Proc. Natl. Acad. Sei. USA, 54, 1552-1557.
Russell W.L, Russell L.В., Kelly E.M. (1958). Radiation dose rate and mutation frequency, Science, 128, 1546-1550.
Russell L.B., Saylors C.L. (1963). The relative sensitivity of various germ cell stages of the mouse to radiation-induced nondisjunction, chromosome losses and deficiency. In: Sobels F. H. (ed.), Repair from genetic damage and differential radiosensitivity in germ cells, Pergamon, Oxford, pp. 313-340.
Salk D. (1982). Werner's syndrome: A review of recent research with an analysis of connective tissue metabolism, growth control of cultures cells and chromosomal aberrations, Num. Genet., 62, 1-15.
Sasaki M.S., Miyata H. (1968). Biological dosimetry in atomic bombs survivors, Nature, 220, 1189-1193.
Satoh C., Awa A.A., NeelJ.V., SchullW.L, Kato H., Hamilton H.B., Otake M., Goriki K. (1982). Genetic effects of atomic bombs, In: Human Genetics, Part A. The Unfolding Genome, Boné-Tamir B. (éd.), A Liss, New York, pp. 267-276.
Searle A. G. (1972). Spontaneous frequencies of point mutations in mice, Hum. Genet., 16, 33-38.
Sergeyev A. S. (1975). On mutation rate of neurofibromatosis, Hum. Genet., 28, 129-138.
de Serres F. J., Mailing H. V. (1969). Identification of the gene alteration in spesific locus mutants at the molecular level, Jpn. J. Genet, 44, 106-113.
Sherman S.L, Morton N.E., Jacobs P.A., Turner G. (1984). The marker (X) syndrome: A cytogenetic and genetic analysis. Ann. Hum. Genet, 48, 21-37.
Sigler A.T., lilienfeld A.M., Cohen B.-H., Westlake J. E. (1965). Radiation exposure in parents with mongolism (Down's syndrome), Johns Hopkins, Med. J., 117, 374.
Sillence D.O. (1983). Disorders of bone density, volume and numeralization. In: Principles and practice of medical genetics (Emery, AEH, Rimoin D. L., eds.), Churchill Livingstone, Edinburgh etc. pp. 736-751.
Sugimura T., Kondo S., Takebe H. (eds.) (1982). Environmental mutagens and carcinogens, Proc. 3rd Intern. Conf. Environmental Mutagens, University of Tokyo Press, A. Liss, Tokyo and New York.
Sutherland G.R. (1982). Heritable fragile sites on human chromosomes. VIII. Preliminary population cytogenetic data on the folic acid sensitive fragile sites, Am. J. Hum. Genet, 34, 452-458.
Swift M. (1982). Disease prediposition of ataxia-teleangiectasia hétérozygotes. In: Ataxia teleangiectasia-a cellular and molecular
296 Литература
link between cancer, neuropathology and immune deficiency, Bridges A., Harnden D. G. (eds.), John Wiley and Sons, New York.
Swift M., Chase Ch. (1979). Cancer in families with xeroderma pigmentosum, J. Natl. Cancer Inst., 62, 1415-1421.
Swift M., Sholman L, Perry M., Chase Ch. (1976). Malignant neoplasms in the families of patients with Ataxia-teleangiectasia, Cancer Res., 36, 209-215.
Szilard L. (1959). On the nature of the ageing process, Proc. Natl. Acad. Sei. USA, 45, 30-45.
Schappert-Kimmijser J., Hemmes G.D., Nijland R. (1966). The heredity of retinoblastoma. In: 2nd Congress of European Society of Ophthalmology, Vienna, 1964, Ophthalmologica, 151, 197-213.
Schmidt H. (1973). Wahrscheinliche genetische Belastung der Bevölkerung mit INH (Isonikotinsäure-Hydrazid), Hum. Genet., 20, 31-45.
Schneider E. L, Mitsui Y. (1976). The relationship between in vitro cellular ageing and in vivo human age, Proc. Nat. Acad. Sei. USA, 73, 3584-3588.
Schnyder U. W. (1966). Tumoren der Haut in genetischer Sicht, Praxis, 55, 1478-1482.
Schölte P. J. L, Sobels F.H., (1964). Sex ratio shift among progeny from patients having received therapeutic X-radiation, Am. J. Hum. Genet., 16, 26-37.
Schroeder T. M. (1972). Genetische Factoren der Krebsentstehung, Forster Med., 16, 603-608.
Schroeder T. M. (1982). Genetically determined chromosome instability syndromes, Cytogenet. Cell Genetics, 33, 119-132.
Schroeder T.M., Anschütz F., Knapp A. (1964). Spontane Chromosomenaberrationen bei familiärer Panmyelopathie, Hum. Genet, 1, 194-196.
Schroeder T. M., Drings P., Beilner P., Buchinger G. (1976). Clinical and cytogenetic observations during a six-year period in an adult with Fanconi's anaemia, Blut, 34, 119-132.
Schroeder T. M., Kurth R. (1971). Analytical review. Spontaneous chromosomal breakage and high incidence of leukemia in inherited disease, Blood, 37, 96.
Schroeder T.M., Tilgen D., Krüger J., Vogel F. (1976). Formal genetics of Fanconi's anemia, Hum. Genet., 32, 257-288.
SchullW.J., NeelJ.V. (1958). Radiation and the sex ratio in man, Science, 128, 343348.
SchullW.J., NeelJ.V., Hashizume A. (1968). Some further observations on the sex ratio among infants born to survivors of the atomic bombings of Hiroshima and Nagasaki, Am. J. Hum. Genet., 18, 328 338.
Schul! W.J., Otake M., Neel J. V. (1981). Genetic effects of the atomic bombs: A reappraisal, Science, 213, 1220-1227.
Stamatoyannopoulos G. (1979). Possibilities for
demonstrating point mutations in somatic cells, as illustrated by studies of mutant hemoglobins. In: Berg K. (ed.), Genetic damage in man caused by environmental agents, Academic Press, New York, pp. 49-62.
Stamatoyannopoulos G., Nute P.E., Miller M. (1981). De novo mutations producing instable hemoglobins or hemoglobin M.I. Establishment of a depository and use data for an association of de novo mutation with advanced parental age, Hum. Genet, 58, 396 404.
Stamatoyannopoulos G., Nute P.E. (1982). De novo mutations producing unstable Hbs or Hbs M. II. Direct estimates of minimum nucleotide mutation rates in man, Hum. Genet, 60, 181-188.
Starlinger P., Saedler H. (1972). Insertion mutations in microorganisms, Biochemie, 54, 177-185.
Stene J., Fischer G., Stene E., Mikkelsen M., Petersen E. (1977). Paternal age effect in Down's syndrome, Ann. Hum. Genet, 40, 299-306.
Stene J., Stene E., Stengel-Rutkowski S., MurkenJ.D. (1981). Parental age and Down's syndrome. Data from prenatal diagnoses (DFG), Hum. Genet, 59, 119-124.
Stevenson A. C. (1957). Achondroplasia: An account of the condition in Northern Ireland, Am. J. Hum. Genet, 9, 81-91.
Stevenson A.C. (1959). The load of heredity defects in human populations, Radiât. Res. [Suppl. 1], 306-325.
Stevenson A. C., Bobrow M. (1967). Determinants of sex proportions in man, with consideration of the evidence concerning a contribution from X-linked mutations to intrauterine death, J. Med. Genet, 4, 190-221.
Stevenson A. C., Kerr C.B. (1967). On the distribution of frequencies of mutation in genes determining harmful traits in man, Mutât. Res., 4, 339-352.
Stribel D., Vogel F. (1958). Ein statistischer Gesichtspunkt für das Planen von Untersuchungen über Änderungen der Mutationsrate beim Menschen, Acta Genet Stat. Med., 8, 274-286.
Tanaka K., Ohkura K. (1958). Evidence of genetic effects of radiation on offspring of radiologic technicians, Jpn. J. Hum. Genet, 3, 135-145.
Taylor A. M. (1963). Bacteriophage - induced mutation in Escherichia colt, Proc. Natl. Acad. Sei. USA, 50, 1043-1051.
IhadaniM.A., Polasa H. (1979). Cytogenetic effects of inactivated influenza virus on male
ferm cells of mice, Hum. Genet, 51, 25358.
Timofeeff-Ressovsky N. W., Zimmer K. G. (1947). Das Trefferprinzip in der Biologie, Leipzig.
TonzO., Glatthaar B. E., Wmterhalter K.H., Ritter H. (1973). New mutation in a Swiss girl leading to clinical and biochemical ß-thalassemia minor, Hum. Genet, 20, 321-327.
Литература 297
Тот О., Winterhalter K. H., Glatthaar В. Е. (1973). New mutation leading to ß-thalassemia minor, Nature, 241, 127.
Tough I. S., Buckton K. E., Baikie A. G., Court Brown W.M. (1960). X-ray induced chromosome damage in man, Lancet, 1960/11, 849-851.
Traut H. (1976). Effects of ionizing radiation on DNA. In: Molecular biology, biochemistry and biophysics, Hüttermann J., Köhnlein W., Téoule R. (eds.), Vol. XXVII, Springer, Berlin Heidelberg, New York, pp. 335-347.
Trimble B.K., Doughty J.H. (1974). The amount of hereditary disease in human populations, Ann. Hum. Genet., 38, 199-223.
TunteW., Becker P.E., v. Knarre G. (1967). Zur Genetik der Myositis ossificans progressiva, Hum. Genet., 4, 320-351.
Uchidal.A., Holunga R., lawler C. (1968). Maternal radiation and chromosomal aberrations, Lancet, II, 1045-1049.
Uchida I.A., lee C.P. V., Byrnes E.M. (1975). Chromosome aberrations induced in vitro by low doses of radiation: Nondisjunction in lymphocytes of young adults, Am. J. Hum. Genet., 27, 419-429.
Van DykeD.L, Weiss L, Roberson J.R., Babu V.R. (1983). The frequency and mutation rate of balanced autosomal rearrangements in man estimated from prenatal genetic studies for advanced maternal age, Am. J. Hum. Genet., 35, 301-308.
Vijayalaxmi Evans H. J., Ray J. H., German J. (1983). Bloom's syndrome: Evidence for an increased mutation frequency in vivo, Science, 221, 851-853.
1666a. Vijayalakshmi Wunder E., Schroeder T.M. (1985). Spontaneous 6-thioguanine-resistant lymphocytes in Fanconi anemia patients and their heterozygous parents, Hum. Genet, 70, 264-270.
Vogel F. (1954). Über Genetic and Mutationsrate des Retinoblastoms (Glioma retinae), Z. Menschl. Vererbungs-Konstitutionslehre, 32, 308-336.
Vogel F. (1956). Über die Prüfung von Modellvorstellungen zur spontanen Mutabilität an menschlichen Material, Z. Menschl. Vererbungs-Konstituonslehre, 33, 470-491.
Vogel F. (1957). Neue Untersuchungen zur Genetik des Retinoblastoms (GÎioma retinae), Z. Menschl. Vererbung-Konstitutionslehre, 34, 205-236.
Vogel F. (1958). Gedanken über den Mechanismus einiger spontaner Mutationen beim Menschen, Z. Menschl. Vererbungs-Konstitutionslehre, 32, 389-399.
Vogel F. (1965). Sind die Mutationsraten für die X-chromosomal rezessiven Hämophilieformen in Keimzellen von Frauen niedriger als in Keimzellen von Männern? Hum. Genet, I, 253-263.
Vogel F. (1970). Monitoring of human populations. In: Chemical mutagenesis in mammals and man, Vogel F., Röhrborn G. (eds.), Sprin-
ger, Berlin, Heidelberg, New York, pp. 445-452.
Vogel F. (1970). Spontaneous mutation in man. In: Chemical mutagenesis in mammals and man, Vogel F., Röhrborn G. (eds.), Springer, Berlin, Heidelberg, New York, pp. 16-68.
Vogel F. (1975). Mutations in man. Approaches to an evaluation of the genetic load due to mutagenic agents in the human population, Mutation Res., 29, 263-269.
Vogel F. (1977). A probable sex difference in some mutation rates, Am. J. Hum. Genet, 29, 312-319.
Vogel F. (1979). Genetics of Retinoblastoma, Hum. Genet., 52, 1-54.
Vogel F. (1983). Mutation in Man. In: Emery A. E. H., Rimoin D. L. (eds.), Principles and Practice of Medical Genetics, Churchill Livingstone, Edinburgh etc., pp. 26-48.
Vogel F. (1984). Mutation and selection in the marker (X) syndrome, Ann. Hum. Genet, 48, 327-332.
Vogel F., Altland K. (1982). Utilization of material from PKU-screening programs for mutation screening. In: Bora K. S. (ed.), Proceedings of an International Symposium on chemical mutagenesis, human population monitoring and genetic risk assessment, Progr. in Mut. Res., Vol. 3, Elsevier, Amsterdam, pp. 143-157.
Vogel F., Jäger P. (1969). The genetic load of a human population due to cytostatic agents, Humangenetik, 7, 287-304.
Vogel F., Корин M. (1977). Higher frequencies of transitions among point mutations, J. Mol. Evol., 9, 159-180.
Vogel F., Krüger J., Brondum Nielsen К., Fryns J. P., Schindler D., Schinzel Α., Schmidt Α., Schwinger E. (1985). Recurrent mutation pressure does not explain the prevalence of the marker (X) syndrome, Hum. Genet, 71, 1-6.
Vogel F., Rathenberg R. (1975). Spontaneous mutation in man, Adv. Hum. Genet, 5, 223-318.
Vogel F., Röhrborn G., Hansmann l. (1974). Die Testung von Fremdstoffen auf Mutagenität, Arzneim Forsch, 24, 1665-1677.
Vogelstein B., Fearon E.R., Hamilton S. R., Feinberg A. P. (1985). Use of restriction fragment length polymorphism to determine the clonal origin of human tumors, Science, 227, 642-645.
Vogt P. K. (1983). Onkogene, Verb. Ges. Dtsch. Naturf. und Ärzte, Wiss. Verlagsgesellschaft, Stuttgart, 235-247.
Wais S., Salvati E. (1966). Klinefelter's syndrome and diabetes mellitus, Lancet, II, 747-748.
Warren S. T., Schulz R. Α., Chang С. С., Wade M.H., Troske J.E. (1981). Elevated spontaneous mutation rate in Bloom syndrome fibroblasts, Proc. Natl. Acad. Sei. USA, 78, 3133-3137.
WeechA.A. (1927). Combined acrocephaly and syndactylism occunng in mother and
298 Литература
daughter. A case report, Johns Hopkins Med. J., 40, 73.
Weinberg H.A. (1983). A molecular basis of cancer, Sei. Am. Nov. 1983, 126-142.
Weinberg R. A. (1984). Ras oncogenes and the molecular mechanisms of carcinogenesis, Blood, 64, 1143-1145.
Weinberg W. (1912). Zur Vererbung des Zwergwuchses, Arch. Rassenund Gesellschafts Biol., 9, 710-718.
Weismann A. (1891). Essays upon heredity and kindred biological problems, Vol. I, Claredon Press (1st ed. 1889, 2nd ed. 1891) Oxford.
Weiss R.A., Marshall C.J. (1984). Oncogenes, Lancet, 2, 1138-1142.
WhitfieldH.J.Jr., Martin R. G., Ames B. (1966). Classification of aminotransferase (C gene) mutants in the histidine operon, J. Mol. Biol., 21, 335-355.
Willecke K., Schäfer R. (1984). Human Oncogenes, Hum. Genet., 66, 132-142.
Williams R. T. (1959). Detoxication mechanisms, 2nd ed., Wiley and Sons, New York.
Winkler U. (1972). Spontaneous mutations in bacteria and phages, Hum. Genet., 16, 19-26.
Winter R. M. (1980). Estimation of male to female ratio of mutation rates from carrier detection tests in X-linked disorders, Am. J. Hum. Genet., 32, 582-588.
Winter R. M., Pembrey M. E. (1982). Does unequal crossing over contribute to the mutation rate in Duchenne muscular dystrophy? Amer, J. Med. Genet, 12, 437-441.
Winter R.M., Tuddenham E.G.D., Goldman E., Matthews K. B. (1983). A maximum likelihood estimate of the sex ratio of mutation rates in hemophilia A, Hum. Genet., 64, 156-159.
Yanase T., Hanada M., Seita M., Ohya T, Imamura T., Fujimura T., Kawasaki K., Yamaoka К. (1968). Molecular basis of morbidityfrom a series of studies of hemoglobinopathies in Western Japan, Jpn. J. Hum. Genet., 13, 40-53.
Yanofsky C., Ito J., Horn V. (1966). Amino acid replacements and the genetic code, Cold. Spring Harbor Symp. Quant. Biol., 31, 151-162.
YunisJ.J. (1983). The chromosomal basis of human neoplasia, Science, 221, 227-236.
YunisJ.J., Soreng A.L (1984). Constitutive fragile sites and cancer, Science, 226, 1199-1204.
Zakrzewski S., Koch M., Sperling K. (1983). Complementation studies between Fanconi's anemia cells with different DNA repair characteristics, Hum. Genet, 64, 55-57.
Zakrzewski S., Sperling K. (1980). Genetic heterogeneity of Fanconi's anemia demonstrated by somatic cell hybrids, Hum. Genet, 56, 81-84.
Zakrzewski S., Sperling K. (1982). Analysis of heterogeneity in Fanconi's anemia patients of different ethnic origin, Hum. Genet, 62, 321-323.
ZanklH., Zang K.D. (1971). Cytological and
cytogenetical studies on brain tumors. III. PhMike chromosomes in human meningiomas, Hum. Genet, 12, 42-49.
ZinklH., Zang K.D. (1972). Cytological and cytogenetical studieson brain tumors. IV. Identification of the missing G chromosome in human meningiomas as no 22 by fluorescence technique, Hum. Genet, 14, 167-169.
Zankl H., Zang K.D. (1974). Quantitative studies on the arrangement of human metaphase chromosomes II. The association frequency of human acrocentric marker chromosomes, Hum. Genet., 23, 259-265.
Zellweger H., Abbo G., Cuany R. (1966). Satellite association and translocation mongolism, J. Med. Genet, 3, 186-189.