АкушерствоАнатомияАнестезиологияВакцинопрофилактикаВалеологияВетеринарияГигиенаЗаболеванияИммунологияКардиологияНеврологияНефрологияОнкологияОториноларингологияОфтальмологияПаразитологияПедиатрияПервая помощьПсихиатрияПульмонологияРеанимацияРевматологияСтоматологияТерапияТоксикологияТравматологияУрологияФармакологияФармацевтикаФизиотерапияФтизиатрияХирургияЭндокринологияЭпидемиология

Приложение 8. 239 11 страница

Прочитайте:
  1. B)новокаинмен жансыздандыру 1 страница
  2. B)новокаинмен жансыздандыру 2 страница
  3. B)новокаинмен жансыздандыру 3 страница
  4. B)новокаинмен жансыздандыру 4 страница
  5. B)новокаинмен жансыздандыру 5 страница
  6. B)новокаинмен жансыздандыру 6 страница
  7. B)новокаинмен жансыздандыру 7 страница
  8. D. Латеральна огинаюча стегно і стегнова 1 страница
  9. D. Латеральна огинаюча стегно і стегнова 10 страница
  10. D. Латеральна огинаюча стегно і стегнова 2 страница

1575. 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.

1576. 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.

1577. 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.

1578. 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.

1579. Newcombe H.B. (1965). The study of mutation and selection in human populations, Eugen. Rev., 57, 109-125.

1580. 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.

1581. Nielsen J., Sillesen I. (1975). Incidence of chromosome aberration among 11, 148 newborn children, Hum. Genet., 30, 1-12.

1582. 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.

1583. 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.

1584. Nowell P. C., Hungerford D. A. (1960). A minute chromosome in human chronic granulocytic leukemia, Science, 132, 1497.

1585. Oehlkers F. (1943). Die Auslösung von Chromosomenmutationen in der Meiosis durch Einwirkung von Chemikalien, Z. Induktiven Abstammungs-Vererbungslehre, 81, 313341.

1586. 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.

1587. Oertelt R. (1970). Klinisch-genetische Analyse des von Hippel-Lindau-Syndroms: Ausgehend von den Anginoblastomen des Kleinhirns, University of Heidelberg, MD Dissertation.

1588. Ohno S. (1972). Gene duplication, mutation

load, and mammalian genetic regulatory systems, J. Med. Genet., 9, 254.

1589. Pearson M., Rowley J.Z. (1985). The relation of oncogenesis and cytogenetics in leukemia and lymphoma, Ann. Rev. Med., 36, 471-483.

1590. 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.

1594. RatnoffO.D., Bennett B. (1973). The genetics of hereditary disorders of blood coagulation, Science, 179, 1291-1298.

1595. Reed Т.Е. (1959). The definition of relative fitness of individuals with specific genetic traits, Am. J. Hum. Genet, 11, 137.

1596. 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.

1598. Reith W. (1970). Mutationen zu Hämophilie A. Häufigkeit im Regierungsbezirk Münster and Abhängigkeit von Zeugungsalter, University of Münster, MD Dissertation.

1599. 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.

1600. Röhrborn G. (1965). Über mögliche mutagene Nebenwirkungen von Arzneimitteln beim Menschen, Hum. Genet., I, 205-231.

1601. Röhrborn G., Berrang H. (1967). Dominant lethals in young female mice, Mutât. Res., 4, 231-233.

1602. 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.

1603. 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.

1604. 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.

1605. 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.

1606. 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.

1607. 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.

1608. 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.

1609. 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.

1610. 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.

1611. Russell W.L, Russell L.В., Kelly E.M. (1958). Radiation dose rate and mutation frequency, Science, 128, 1546-1550.

1612. 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.

1613. 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.

1614. Sasaki M.S., Miyata H. (1968). Biological dosimetry in atomic bombs survivors, Nature, 220, 1189-1193.

1615. 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.

1616. Searle A. G. (1972). Spontaneous frequencies of point mutations in mice, Hum. Genet., 16, 33-38.

1617. Sergeyev A. S. (1975). On mutation rate of neurofibromatosis, Hum. Genet., 28, 129-138.

1618. 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.

1619. 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.

1620. 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.

1621. 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.

1622. 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.

1623. 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.

1624. 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.

1625. Swift M., Chase Ch. (1979). Cancer in families with xeroderma pigmentosum, J. Natl. Cancer Inst., 62, 1415-1421.

1626. Swift M., Sholman L, Perry M., Chase Ch. (1976). Malignant neoplasms in the families of patients with Ataxia-teleangiectasia, Cancer Res., 36, 209-215.

1627. Szilard L. (1959). On the nature of the ageing process, Proc. Natl. Acad. Sei. USA, 45, 30-45.

1628. 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.

1629. Schmidt H. (1973). Wahrscheinliche genetische Belastung der Bevölkerung mit INH (Isonikotinsäure-Hydrazid), Hum. Genet., 20, 31-45.

1630. 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.

1631. Schnyder U. W. (1966). Tumoren der Haut in genetischer Sicht, Praxis, 55, 1478-1482.

1632. 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.

1633. Schroeder T. M. (1972). Genetische Factoren der Krebsentstehung, Forster Med., 16, 603-608.

1634. Schroeder T. M. (1982). Genetically determined chromosome instability syndromes, Cytogenet. Cell Genetics, 33, 119-132.

1635. Schroeder T.M., Anschütz F., Knapp A. (1964). Spontane Chromosomenaberrationen bei familiärer Panmyelopathie, Hum. Genet, 1, 194-196.

1636. 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.

1637. Schroeder T. M., Kurth R. (1971). Analytical review. Spontaneous chromosomal breakage and high incidence of leukemia in inherited disease, Blood, 37, 96.

1638. Schroeder T.M., Tilgen D., Krüger J., Vogel F. (1976). Formal genetics of Fanconi's anemia, Hum. Genet., 32, 257-288.

1639. SchullW.J., NeelJ.V. (1958). Radiation and the sex ratio in man, Science, 128, 343348.

1640. 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.

1641. Schul! W.J., Otake M., Neel J. V. (1981). Genetic effects of the atomic bombs: A reappraisal, Science, 213, 1220-1227.

1642. 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.

1643. 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.

1644. 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.

1645. Starlinger P., Saedler H. (1972). Insertion mutations in microorganisms, Biochemie, 54, 177-185.

1646. Stene J., Fischer G., Stene E., Mikkelsen M., Petersen E. (1977). Paternal age effect in Down's syndrome, Ann. Hum. Genet, 40, 299-306.

1647. 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.

1648. Stevenson A. C. (1957). Achondroplasia: An account of the condition in Northern Ireland, Am. J. Hum. Genet, 9, 81-91.

1649. Stevenson A.C. (1959). The load of heredity defects in human populations, Radiât. Res. [Suppl. 1], 306-325.

1650. 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.

1651. 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.

1652. 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.

1653. Tanaka K., Ohkura K. (1958). Evidence of genetic effects of radiation on offspring of radiologic technicians, Jpn. J. Hum. Genet, 3, 135-145.

1654. Taylor A. M. (1963). Bacteriophage - induced mutation in Escherichia colt, Proc. Natl. Acad. Sei. USA, 50, 1043-1051.

1655. IhadaniM.A., Polasa H. (1979). Cytogenetic effects of inactivated influenza virus on male

f

erm cells of mice, Hum. Genet, 51, 25358.

1656. Timofeeff-Ressovsky N. W., Zimmer K. G. (1947). Das Trefferprinzip in der Biologie, Leipzig.

1657. 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


1658. Тот О., Winterhalter K. H., Glatthaar В. Е. (1973). New mutation leading to ß-thalassemia minor, Nature, 241, 127.

1659. 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.

1660. 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.

1661. Trimble B.K., Doughty J.H. (1974). The amount of hereditary disease in human populations, Ann. Hum. Genet., 38, 199-223.

1662. TunteW., Becker P.E., v. Knarre G. (1967). Zur Genetik der Myositis ossificans progressiva, Hum. Genet., 4, 320-351.

1663. Uchidal.A., Holunga R., lawler C. (1968). Maternal radiation and chromosomal aberrations, Lancet, II, 1045-1049.

1664. 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.

1665. 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.

1666. 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.

1667. Vogel F. (1954). Über Genetic and Mutationsrate des Retinoblastoms (Glioma retinae), Z. Menschl. Vererbungs-Konstitutionslehre, 32, 308-336.

1668. Vogel F. (1956). Über die Prüfung von Modellvorstellungen zur spontanen Mutabilität an menschlichen Material, Z. Menschl. Vererbungs-Konstituonslehre, 33, 470-491.

1669. Vogel F. (1957). Neue Untersuchungen zur Genetik des Retinoblastoms (GÎioma retinae), Z. Menschl. Vererbung-Konstitutionslehre, 34, 205-236.

1670. Vogel F. (1958). Gedanken über den Mechanismus einiger spontaner Mutationen beim Menschen, Z. Menschl. Vererbungs-Konstitutionslehre, 32, 389-399.

1671. 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.

1672. 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.

1673. 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.

1674. 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.

1675. Vogel F. (1977). A probable sex difference in some mutation rates, Am. J. Hum. Genet, 29, 312-319.

1676. Vogel F. (1979). Genetics of Retinoblastoma, Hum. Genet., 52, 1-54.

1677. 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.

1678. Vogel F. (1984). Mutation and selection in the marker (X) syndrome, Ann. Hum. Genet, 48, 327-332.

1679. 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.

1680. Vogel F., Jäger P. (1969). The genetic load of a human population due to cytostatic agents, Humangenetik, 7, 287-304.

1681. Vogel F., Корин M. (1977). Higher frequencies of transitions among point mutations, J. Mol. Evol., 9, 159-180.

1682. 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.

1683. Vogel F., Rathenberg R. (1975). Spontaneous mutation in man, Adv. Hum. Genet, 5, 223-318.

1684. Vogel F., Röhrborn G., Hansmann l. (1974). Die Testung von Fremdstoffen auf Mutagenität, Arzneim Forsch, 24, 1665-1677.

1685. 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.

1686. Vogt P. K. (1983). Onkogene, Verb. Ges. Dtsch. Naturf. und Ärzte, Wiss. Verlagsgesellschaft, Stuttgart, 235-247.

1687. Wais S., Salvati E. (1966). Klinefelter's syndrome and diabetes mellitus, Lancet, II, 747-748.

1688. 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.

1689. WeechA.A. (1927). Combined acrocephaly and syndactylism occunng in mother and


298 Литература


daughter. A case report, Johns Hopkins Med. J., 40, 73.

1690. Weinberg H.A. (1983). A molecular basis of cancer, Sei. Am. Nov. 1983, 126-142.

1691. Weinberg R. A. (1984). Ras oncogenes and the molecular mechanisms of carcinogenesis, Blood, 64, 1143-1145.

1692. Weinberg W. (1912). Zur Vererbung des Zwergwuchses, Arch. Rassenund Gesellschafts Biol., 9, 710-718.

1693. Weismann A. (1891). Essays upon heredity and kindred biological problems, Vol. I, Claredon Press (1st ed. 1889, 2nd ed. 1891) Oxford.

1694. Weiss R.A., Marshall C.J. (1984). Oncogenes, Lancet, 2, 1138-1142.

1695. 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.

1696. Willecke K., Schäfer R. (1984). Human Oncogenes, Hum. Genet., 66, 132-142.

1697. Williams R. T. (1959). Detoxication mechanisms, 2nd ed., Wiley and Sons, New York.

1698. Winkler U. (1972). Spontaneous mutations in bacteria and phages, Hum. Genet., 16, 19-26.

1699. 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.

1700. 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.

1701. 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.

1702. 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.

1703. Yanofsky C., Ito J., Horn V. (1966). Amino acid replacements and the genetic code, Cold. Spring Harbor Symp. Quant. Biol., 31, 151-162.

1704. YunisJ.J. (1983). The chromosomal basis of human neoplasia, Science, 221, 227-236.

1705. YunisJ.J., Soreng A.L (1984). Constitutive fragile sites and cancer, Science, 226, 1199-1204.

1706. Zakrzewski S., Koch M., Sperling K. (1983). Complementation studies between Fanconi's anemia cells with different DNA repair characteristics, Hum. Genet, 64, 55-57.

1707. Zakrzewski S., Sperling K. (1980). Genetic heterogeneity of Fanconi's anemia demonstrated by somatic cell hybrids, Hum. Genet, 56, 81-84.

1708. Zakrzewski S., Sperling K. (1982). Analysis of heterogeneity in Fanconi's anemia patients of different ethnic origin, Hum. Genet, 62, 321-323.

1709. ZanklH., Zang K.D. (1971). Cytological and


cytogenetical studies on brain tumors. III. PhMike chromosomes in human meningiomas, Hum. Genet, 12, 42-49.

1710. 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.

1711. 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.

1712. Zellweger H., Abbo G., Cuany R. (1966). Satellite association and translocation mongolism, J. Med. Genet, 3, 186-189.

Литература к главе 6

1713. Adams M.S., NeelJ.V. (1967). Children of incest, Pediatrics, 40, 55-62.

1714. Allison A.C. (1954). Protection afforded by sickle-cell trait against subtertian malaria infection, Br. Med. J., I, 290.

1715. Allison A.C. (1954). The distribution of the sickle-cell trait in East Africa and elsewhere, and its apparent relationship to the incidence of subtertian malaria, Trans. R. Soc. Trop. Med. Hyg., 48, 312.

1716. Allison A.C. (1954). Notes on sickle-cell polymorphism, Ann. Hum. Genet, 19, 39.

1717. Allison A.C. (1955). Aspects of polymorphism in man, Cold Spring Harbor Symp. Quant. Biol., 20, 239.

1718. Allison A.C. (1956). The sickle and hemoglobin C-genes in some African populations, Ann. Hum. Genet, 21, 678.

1719. Allison A.C. (1964). Polymorphism and natural selection in human populations, Cold Spring Harbor Symp. Quant. Biol., 24, 137-149.

1720. Anonymous (1983). WHO Working Group (including A Motulsky and 13 others): Community control of hereditary anaemias, Bull. WHO, 61, 63-80. Also published in French, Bull. WHO, 61, 277-297.

1721. Antonarakis S.E., Boehm C.D., Serjeant G.R., Theisen C.E., Dover G.J., KazazianH.H. (1984). Origin of the ß-globin gene in Blacks: The contribution of recurrent mutation or gene conversion or both, Proc. Natl. Acad. Sei. USA, 81, 853-856.

1722. BairdP.A., McGillivray B. (1982). Children of incest, J. Pediatr., 101, 854-857.

1723. Bashi J. (1977). Effects of inbreeding on cognitive performance, Nature, 266, 440-442.

1724. Beet E. A. (1946). Sickle-cell disease in the Balovale district of North Rhodesia, East Afr. Med. J., 23, 75.

1725. Beet E. A. (1947). Sickle-cell disease in Northern Rhodesia, East Afr. Med. J., 24, 212-222.

1726. Bergeron P., laberge C., Grenier A. (1974). Hereditary tyrosinemia in the province of


Литература 299


Quebec: Prevalence at birth and geographic distribution, Clinical Genetics, 5, 157-162.

1727. Bernhard W. (1966). Über die Beziehung zwischen ABO-Blutgruppen und Pockensterblichkeit in Indien und Pakistan, Homo, 17, 111.

1728. Block J. (1901). Der Ursprung der Syphilis, Fischer, Jena.

1729. Blumberg B.S., Hesser J.E. (1971). Loci differently affected by selection in two American black populations, Proc. Natl. Acad. Sei. USA, 68, 2554.

1730. Bois E., Feingold J., Demenais F., Runavot Y., Jehanne M., Toidic L (1978). Cluster of cystic fibrosis cases in a limited area of Brittany (France), Clin. Genet., 14. 73-76.

1731. Bosnjakovic S. (1938). Vererbungsverhaltnise bei der sogenannten Krankheit von Mljet, Acta Derm. Venereol. (Stockh.), 19, 88.

1732. BruesA.M. (1954). Selection and polymorphism in the ABO blood groups, Am. J. Phys. Anthropol., 12, 559-598.

1733. Cam R.L, Brown W.M., Wilson A.C. (1984). Polymorphic sites and the mechanism of evolution in human mitochondrial DNA, Genetics, 106, 479-499.

1734. Carter C. O. (1967). Risk of offspring of incest, Lancet, I, 436.

1735. Cavalli-Sforza L. L., Edwards A. W. F. (1967). Phylogenetic analysis: Models and estimations procedures, Evolution, 21, 550-570.

1736. Cerimele D., Cottoni F., Scappaticci S., Rabbiosi G., Sanna E., Zei G., Fraccaro M. (1982). High prevalence of Werner's syndrome in Sardinia. Description of six patients and estimate of the gene frequency, Hum. Genet, 62, 25-30.

1737. ChakravarttiM.R., Vogel F. (1971). Haemaglutinatior-inhibiting variola antibodies in blood serum of former smallpox-patients, their healthy siblings and unvaccinated controls in other areas, Humangenetik, 11, 336-338.

1738. Charnov E. (1977). An elementary treatment of kin selection, J. Theor. Biol., 66, 541-550.

1739. Clarke B. (1975). Frequency-dependent and density-dependent natural selection. In: The role of natural selection in human evolution, Salzano F. (ed.), North Holland, American Elsevier, Amsterdam, New York, pp. 187-200.

1740. Clarke LA. (1974). Rh haemolytic disease, Original papers commentaries, Medical and Technical Publ. Сотр., Newcastle.

1741. Comings D.E. (1982). Two-dimensional gel electrophoresis of human brain proteins. III. Genetic and non-genetic variations in 145 brains, Clin. Chem., 28, 798-804.

1742. Cooper D. N.. Smith B. A., Cooke H.J., Niemann S., Schmidtke J. (1985). An estimate of unique DNA sequence heterozygosity in the human genome, Hum. Genet., 69, 201-205.


Дата добавления: 2015-12-16 | Просмотры: 425 | Нарушение авторских прав







При использовании материала ссылка на сайт medlec.org обязательна! (0.031 сек.)