 |
|
АкушерствоАнатомияАнестезиологияВакцинопрофилактикаВалеологияВетеринарияГигиенаЗаболеванияИммунологияКардиологияНеврологияНефрологияОнкологияОториноларингологияОфтальмологияПаразитологияПедиатрияПервая помощьПсихиатрияПульмонологияРеанимацияРевматологияСтоматологияТерапияТоксикологияТравматологияУрологияФармакологияФармацевтикаФизиотерапияФтизиатрияХирургияЭндокринологияЭпидемиология |
Приложение 8. 239 3 страница221. Weatherall D.J. (1985). The New Genetics and Clinical Practice, Oxford Univ. Press. 222. Weatherall D.J., CleggJ.B. (1981). The Thalassemia Syndromes, 3rd ed., Blackwell., Oxford. m. White M. J.D. (1973). Animal cytology and evolution, 3rd ed., Cambridge University Press, New York. 224. Wiedemann Я.-Λ, Grosse F.-R., Dibborn H. (1982). Das charakteristische Syndrom, Schattauer, Stuttgart, New York. 225. Williams R.J. (1956). Biochemical individuality, John Wiley and Sons, New York. 226. Wolpert L. (1984). DNA and its message, Lancet, 2, 853-856. 227. Wood C., Trounson A. (1984). Clinical in vitro fertilization, Springer, Berlin etc. 228. Work T.S., Burden R.H., (eds.) (1983). Laboratory techniques in biochemistry and molecular biology, Elsevier, Amsterdam, New York, Oxford. 229. Wyngaarden J.B., Smith L.H. (eds.) (1985). Cecil Textbook of Medicine, Sauders, Philadelphia. 230. Yunis J.J. (ed.) (1969). Biochemical methods in red cell genetics, Academic Press, New York, London. 231. Yunis J.J. (ed.) (1979). Chromosomal Syndromes, Academic Press, New York. 232. Zacharov A. F., Benusch V. A., Kuleshov N. P., Baranowskaya L.I. (in Russian) (1982). Human Chromosomes (Atlas), Meditsma, Moscow. 233. Zaleski M.B., Dubiski S., Niles E.G., Cunningham R.K. (1983). Immunogenetics, Pitman, Boston etc. 234. Zerbin-Rüdin E. (1967). Hirnatrophische Prozesse. In: Becker P. E. (ed.), Humangenetik, ein kurzes Handbuch, Vol. П/2, pp. 84 157, Thieme Verlag, Stuttgart. 235. Züblin W. (1969). Chromosomale Aberration und Psyche, Karger, Basel, New York. Литература к введению и главе 1 236. Allen G.E. (1975). Genetics, eugenics and class struggle, Genetics, 79, 29 45. 236a.Becker P. E. Wege ins dritte Reich, Wissenschaftler und Ideologen vor Hitler (To be printed). 237. Cairns J., S tent G.S., Watson J.D. (1966). Phage and the origin of molecular biology, Cold Spring Harbor Lab., New York. 238. Committee for the Study of Inborn Errors of Metabolism, Assembly of Life Sciences NRC, Genetic screening. Programs, principles, and research, National Academy of Sciences 1975, Washington (D.C). 239. Baltzer F. (1962). Theodor Boveri-Leben und Werk. Wissenschaftliche Verlagsgesellschaft, Stuttgart. 240. Bernstein F. (1924). Ergebnisse einer biostatistischen zusammenfassenden Betrachtung über die erblichen Blutstrukturen des Menschen, Klin. Wochenschr., 3, 1495-1497. 241. Bodmer W. F. (ed.) (1978). The HLA system, Br. Med. Bull., 34, (3), 213-319. 242. Brock D. J. H. (1977). Biochemical and cytological methods in the diagnosis of neural tube defects, Prog. Med. Genet., 2, 1-40. 243. Bunge M. (1967). Scientific research. I. The search for system. II. The search for truth, Springer, Berlin, Heidelberg, New York. 244. Capelle W. (1953). Die Vorsokratiker, Knöner, Stuttgart. 244a.Cremer T. (1986). Von der Zellenlehre zur Chromosomentheorie, Springer, Berlin etc. 245. Dungern E. von, Hirszfeld L. (1911). On the groupspecific structures of the blood. III. Z. Immunitatsforsch., 8, 526-562. 246. Dunn L. C. (1962). Cross current in the history of human genetics, Am. J. Hum. Genet, 14, 1-13. 247. Ephrussi В., Weiss M. C. (1965). Interspecific hybridization of somatic cells, Proc. Natl. Acad. Sei. USA, 53, 1040. 247a.Fa/fe R. (1984). The gene in search of an identity, Hum. Genet., 68, 195-204. 248. Gallon F. (1865). Hereditary talent and character, Macmillan's Magazine, 12, 157. 254 Литература 249. Garrod A. E. (1902). The incidence of alcaptonuria: A study in chemical individuality, Lancet, II, 1616-1620. 250. Graham L.R. (1977). Political ideology and genetic theory: Russian and Germany in the 1920's, Hastings Cent. Rep., 7, 30-39. 251. Haller M. (1963). Eugenics; hereditarian attitudes in American thought, New Brunswick (NJ). 252. Hardy G.H. (1908). Mendelian proportions in a mixed population, Science, 28, 49-50. 253. Harris H. (1969). Enzyme and protein polymorphism in human populations, Br. Med. Bull., 25, 5. 254. Harris H., WatkinsJ.F. (1965). Hybrid cells from mouse and man: artificial heterokaryons of mammalian cells from different species, Nature, 205, 640. 255. Joravsky D. (1970). The Lysenko affair, Harvard University Press, Boston. 256. Kevles D.J. (1985). In the Name of Eugenics, Genetics and the Uses of Human Heredity, Alfred A. Kopf, New York. 257. Kühn T. S. (1962). The structure of scientific revolutions, University of Chicago Press, Chicago. 258. Lakatos I., Musgrave A. (1970). Criticism and the growth of knowledge, Cambridge University Press, New York. 259. Landsteiner K. (1900). Zur Kenntnis der antifermentativen, lytischen und agglutinierenden Wirkunden des Blutserums und der Lymphe, Zentralbl. Bakteriol, 27, 357-362. 260. Ladsteiner K., Wiener A. S. (1940). An agglutinable factor in human blood recognized by immune sera for rhesus blood, Proc. Soc. Exp. Biol., 43, 223. 261. Levine P., Burnham L., Katzin E. M., Vogel P. (1941). The role of isoimmunization in the pathgenesis of erythroblastosis fetalis, Am. J. Obstet. Gynecol., 42, 925-937. 262. levine P., Stetson R.E. (1939). An unusual case of intragroup agglutination, J. Am. Med. Assoc., 113, 126-127. 263. Ludmerer K. (1972). Genetics and American society, Johns Hopkins University Press, Baltimore. 264. McKusick V.A. (1975). The growth and development of human genetics as a clinical discipline, Am. J. Hum. Genet., 27, 261-273. 265. Medvedev Z. (1977). Soviet genetics: new controversy, Nature, 268, 285-287. 266. Mendel G.J. (1865). Versuche über Pflanzenhybriden, Verhandlungen des Naturforschenden Vereins (Brunn.). 267. Mohr H. (1977). The structure and significance of science, Springer, New York, Heidelberg, Berlin. 268. Motulsky A. G. (1959). Joseph Adams (17561818). Arch. Intern. Med., 104, 490-496. 269. Motylsky A. G. (1972). History and current Status of pharmacogenetics. In: Human Genetics: Proceedings of the 4th International Congress of Human Genetics, Paris, September 1971, pp. 381-390, Excerpta Medica, Amsterdam. 270. Motulsky A. G. (1978). The genetics of common diseases. In: Morton N. E., Chung C. S. (eds.), Genetic epidemiology, pp. 541-548, Academic Press, New York. 210n.Motulsky A. G. (1984). Genetic Epidemiology, Genet. EpidemioL, I, 143-144. 271. Motulsky A.G. (1977). Ecogenetics: genetic variation in susceptibility to environmental agents. In: Human Genetics: Proceedings of the 5th International Congress of Human Genetics, Mexico City, 10-15 October 1976, pp. 375-385, Excerpta Medica, Amsterdam. 272. Motulsky A. G. (1978). Presidential address: Medical and human genetics 1977: trends and directions, Am. J. Hum. Genet, 30, 123-131. 272a.Muller~Hill B. (1984). Todliche Wissenshaft, Rowohlt, Hamburg. 273. Nachtsheim H. (1952). Für und wider die Sterilisierung aus eugenischer Indikation, Thieme, Stuttgart. 274. Nasse C. F. (1820). Von einer erblichen Neigung zu tödlichen Blutungen, p. 385, Horns Archiv. 275. N eel J. V. (1966). Between two worlds, Am. J. Hum. Cenet., 18, 3-20. 276. Penrose L.S. (1967). Presidential Address-the influence of the Inglish tradition in human genetics. In: Crow J. E., Neel J. V. (eds.). Proceedings of the 3rd International Congress of Human Genetics, pp. 13-25, Johns Hopkins University Press, Baltimore. 277. Ploetz A. (1895). Die Tüchtigkeit unserer Rasse und der Schutz der Schwachen: Ein Versuch über Rassenhygiene und ihr Verhältnis zu den humanen Idealen, besonders zum Sozialismus, S. Fischer, Berlin. 278. Pollack W., Gorman J. C., Freda V.J. (1969). Prevention of Rh hemolytic disease. In: Brown E, Moore C. V. (eds.), Progress in Hematology. VI. Vol. VI, pp. 121-147, Heinemann Medical Books, London. 279. Popper K. R. (1970). Normal science and its dangers. In: Lakatos L, Musgrave A. (eds.), Criticism and the growth of knowledge, pp. 51-58, Cambridge University Press, New York. 280. Popper K. R. (1934). Logik der Forschung, Mohr, Tubingen (4rd ed. 1971). 281. Popper K. R. (1963). Conjectures and refutations, Rutledge and Kregan Paul, London. 282. Reitlinger G. (1961). The final solution, Barnes, New York. 283. Rosenberg C.E. (1976). No other dogs. On science and American social thought, Johns Hopkins University Press, Baltimore. 284. Rüdin E. (1916). Studien über Vererbung und Entstehung geistiger Störungen. I. Zur Vererbung und Neuentstehlung der Dementia praecox, Springer, Berlin. 285. Standury J.B. (1974). Inborn errors of the thyroid, Progr. Med. Genet., 10, 55-80. 286. Versöhner O. von (1937). Was kann der Historiker, der Genealoge und der Statistiker zur Erforschung des biologischen Problems der Judenfrage beitragen? Forschungen zur Judenfrage, 2, 216-222. Литература 255 !87. Watkins J.W.N. (1970). Agains "normal science". In: Lakatos I., Musgrave A. (eds.), Criticism and the growth of knowledge, pp. 25-38, Canblidge University Press, New York. !88. Weinberg W. (1901). Beiträge zur Physiologie und Pathologie der Mehrlingsgeburten beim Menschen, Arch. Ges. Physiol., 88, 346-430. !89. Weinberg W. (1908). Über den Nachweis der Vererbung beim Menschen, Jahreshelfte des Vereins für vaterländische Naturkunde in Württemberg, 64, 368-382. !90. Weinberg W. (1912). Weitere Beiträge zur Theorie der Vererbung. IV. Über Methode und Fehlerquellen der Untersuchung auf Mendelsche Zahlen beim Menschen, Arch. Rass, Ges. Biol, 9, 165-174. !91. Zimmerman D. (1973). Rh. The intimate history of a disease and its conquest, p. 371, Macmillan, New York. Литература к главе 2 Ш. Aller V., AlbisquetaJ.A., Perez Α., Martin M. Α., Goday С., Del Mazo J. (1975). A case of trisomy 8 mossaicism 47, XY, +8/46, XX, Clin. Genet., 7, 232-237. Ï93. Anderson S., Bankier A. T., Barrel B.C., de Bruyn M. H. L., Coulson A. R., Dramin J., Eperon I. C., Nierlich O.P., Rue S.A., Sanger F., Schreier P. H., Smith A. J. H., Staden R., Young I.G. (1981). Science and organization of the human mitochondrial genome, Nature, 290, 457-465. !94. Angell R.R., Hitken R.J., van Look P.P. A., LumsdenM.A., Templeton A.A. (1983). Chromosome abnormalities in human embryos after in vitro fertilization, Nature, 303, 336-338. 295. Appelhans H., Vosberg H.-P. (1984). Characterization of a human genomic DNA fragment coding for a myosin heavy chain, Hum. Genet. 296. Arber W. (1979). Promotion and limitation of genetic exchange, Science, 205, 361-365. 297. Arnold J. (1879). Beobachtungen über Kernteilungen in den Zellen der Geschwulste, Virchows Arch. [Pathol. Anat.], 78, 279. Wa.BalkanW., Martin R. H. (1983). Chromosome segreration into the spermatozoa of two men heterozygous for different regional translocations, Hum. Genet., 63, 345-348. 298. Ban M.L., Bertram L.F. (1949). A morphological distinction between neurones of the male and the female and the behavior of the nucleolar satellite during accelerated nucleoprotein synthesis, Nature, 163, 676-677. 299. Berg P. (1981). Dissections and reconstructions of genes and chromosomes, Science, 213, 296-303. 300. Berger R., Tonati G., Dene J., Ortiz Μ. Α., MartinelliJ. (1974). Cri du chat syndrome with maternal insertional translocation, Clin. Genet, 5, 428-432. 301. Bergsma D. (ed.) (1974). Urinary system and others, Birth Defects, 10, (4), Part XVI, Williams and Wilkins, Baltimore.
302. Beutler E. (1963). Autosomal inactivation, Lancet, I, 1242. 303. Beutler E. (1964). Gene inactivation: The distribution of gene products among popoulations of cells in heterozygous humans, Cold. Spring Harbor Symp. Quant. Biol., 29, 261. 304. Beutler F., Yeh M., Fairbanks V.F. (1962). The normal human female as a mosaic of X chromosome activity: Strudies using the gene for G-6-PD as a marker, Proc. Natl. Acad. Sei. USA 48 9 305. Blanc h'., ChenK.-H., D'Amore M.A., Wallace D. C. (1983). Amino acid caange associated with the major polymorphic Hinc II site of Oriental and Caucasian Mitochondrial DNAs, Americ. J. Hum. Genet, 35, 167-176. 306. Bochkov N.P., Kuleshov N.P., Cheboratev A.N., AlekhinV.L, MidianS.A. (1974). Population cytogenetic investigation of newborns in Moscow, Hum. Genet, 22, 139-152. 307. Boomer W.F. (1981). The William Allan Memorial Award Adress: Gene clusters, genome organization and complex phenotypes. When the sequence is known, what will it mean? Amer. J. Hum. Genet, 33, 664-682. 308. Book J.A., Santesson B. (1960). Malformation syndrome in man associated with triploidy (69 chromosomes), Lanset, I, 858-859. 309. BornG., Grützner P., Hemminger H.J. (1976). Evidenz für eine Mosaikstruktur der Netzhaut bei Konduktorinnen für Dichromasie, Hum. Genet, 32, 189-196. 310. Boue J., Barichard F., Deluchat C., Der Sarkissian H., Galano P., Boue A. (1981). Diagnostic prenatal des anomalies de la structure chromosomique. 226 observations, La Nouvelle Presse Médicale, 10, 3299-3301. 311. Bridges C.B. (1916). Non-disjunction as proof on the chromosome theory of heredity, Genetics, I, 1-52; 107-163. 312. Brisson N.. Verma D.P.S. (1982). Soybean leghemoglobin gene family: Normal, pseudo, and truncated genes, Proc. Natl. Acad. Sei. USA, 79, 4055-4059. 313. Brown S.W. (1966). Heterochromatin, Science, 151, 417-435. 314. Brownlee G.G., Rizza A. (1984). Clotting factor VIII cloned, Nature, 312, 307. 315. Bühler E. M. (1980). A synapsis of the human Y chromosome, Hum. Genet, 55, 145-175. 3l5a.Burgoyne P.S. (1986). Mammalian X and Y crossover, Nature, 319, 258-259. 316. Cerr D. H. (1970c). Chromosome studies in selected spontaneous a abortions. I. Conception after oral contraceptives, Can. Med. Assoc. J., 103, 343-348. 317. Can D.H. (1971). Chromosomes and abortion, Adv. Hum. Genet, 2, 201-257.
318. Can D.H. (1967). Chromosome anomalies as a cause of spontaneous abortion, Am. J. Obstet. GynecoL, 97, 283. 319. Carter CO., Hamerton J.L., Polani P.E., Gunalp A., Weiler S. D. V. (1960). Chromosome translocation as a cause familian mongolism, Lancet, Π, 678-680. Литература 320. Caspersson T., de la Chapelle S., Foley G. E., Kudynowski J., Modest E. J., Simonsson E., Wagh V., Zecht L. (1968). Chemical differentiation along metaphase chromosomes, Exp. Cell. Res., 49, 219. 321. Cattanach В. M. (1975). Control of chromosome inactivation, Ann. Rev. Genet., 9, 1-18. 322. Chadefaux В., Allord D., Rethoré M. О., Raoul О., Poissonier M., Gilgenkrautz S., Cheruy C., Jérôme H. (1984). Assignment of Human phosphoribosylglycinamide synthetase locus to region 21q 22.1. Hum. Genet, 66, 190-192. 323. Chapelle A. de la, Schröder J., Stensand K., Felhnan J., Herva R., Saarni M., Auttonainen L, Tallila L., Tervilae L., Husa L., Tallquist G., RobsonE.B., CookP.J.L., Sanger R. (1974). Pericentric inversion of human chromosomes 9 and 10, Am. J. Hum. Genet., 26, 746-765. 324. Clendenin T.M., Benirschke K. (1963). Chromosome studies on spontaneous abortions, Lab. Invest, 12, 1281-1292. 325. Cohen M. M., Shaw M. W. (1964). Effects of mitomycin С on human chromosomes, J. Cell. Biol., 23, 386-395. 326. Cohen M. M. (1971). The chromosomal constitution of 165 human translocations involving D group chromosomes identified by autoradiography, Am. Genet (Paris), 14, 87-96. 327. Collman R.D., Stoller A. (1963). A life table for mongols in Victoria, J. Ment Defic. Res., 7, 53. 328. Cooper D.N., Scgmidtke J. (1984). DNA restriction fragment length polymorphism and heterozygosity in the human genome. Hum. Genet, 66, 1-16. 328a.Cooper D.N., Schmidtke J. (1986). Diagnosis of genetic disease using recombinant DNA, Hum. Genet, 73, 1-11. 329. Creasy M.R., Crolla J.A., Alberman E.D. (1976). A cytogenetic study of human spontaneous abortions using banding techniques, Hum. Genet, 31, 177-196. 330. Cremer С., Cray J. W., Ropers H.-H. (1982). Flow cytometric charactirization of a Chinese hamster χ man hybrid cell line retaining the human Y chromosome, Hum. Genet, 60, 262-266. 331. Davidson W.M., Smith D.R. (1954). The nuclear sex of leucocytes. In: Overzier (ed.), Intersexuality, pp. 72-85, Academic Press, New York. 332. Davies K.E. (1981). The applications of DNA recombinant technology to the analysis of the human genome and genetic disease, Hum. Genet, 58, 351-357. 333. Davies K. E., Young B. D., Elles R. G., Hill M. E., Williamson R. (1981). Cloning of a representative genomic library of the human X chromosome after sorting by flow cutometry, Nature, 293, 374-375. 334. Davis J. R., Rogers В. В., Hageman R. M., IhiesC.A., Veomett l.C. (1985). Balanced reciprocal translocations: risk factors for aneuploid segregant viability, Clin., Genet, 27, 1-19. 335. DelhantyJ.A., Ellis J.R., Rowley P. T. (1961). Triploid cells in a human embryo, Lancet, I, 1286. 336. Denaro M., Blanc H., Johnson M.J., Chen K.H., Wilmsen E., Cavalli-Sforza L. L., Wallace D. C. (1981). Ethnic variation in Hp I endonuclease cleavage patterns of human mitochondrial DNA, Proc. Natl. Acad. Sei. USA, 78, 5768-5772. 337. Drets M.E., Shaw M. W. (1971). Specific banding patterns of human chromosomes, Proc. Natl. Acad. Sei. USA, 68, 2073. 338. Ducos J., Marty Y., Sanger R, Rece R. R. (1971). Xg and X chromosome inactivation, Lancet, П, 219-220. 339. Dutrillaux B. (1973). Nouveau système de marquage chromosomique: Les bandes T. Chromosoma, 41, 395. 340. Dutrillaux В., Laurent C., Robert J. M., Lejeune J. (1973). Inversion péricentrique, inv (10), chez la mère et aneusomie de recombinaison, inv (10), rec (10), chez son fils, Cytogenet Cell Genet, 12, 245-253. 341. Dutrillaux В., Lejeune J. (1975). New techniques in the study of human chromosomes: Methods and applocations, Adv. Hum. Genet, 5, 119 156. 342. Dutrillaux В., Viegas-Péguignot E., Aurias Α., Mouthuy M., Prieur M. (1981). Non random position of metaphasic chromosomes: A study of radiation induced and constitutional chromosome rearrangements, Hum. Genet, 59, 208-210. 343. Edwards J.H., HarndenJ.C., Cameron A. H., Crosse V.M., Wolff Ο. Η. (1960). A new trisomie syndrome, Lancet, I, 787. 344. Engel J., Gunning P., Kedes L. (1982). Human actin proteins as encoded by a multigene family. In: Pearson M. L., Epstein H. F. (eds), Muscle development, molecular ans cellular control, pp. 107-117, Cold Spring Harbor Lab. Cold Sprind Harbor, New York. 345. Epstein C.J. (1969). Mammalian oocytes: X chromosome activity, Science, 163, 1078. 346. Evans H.J. (1977). Chromosome anomalies among livebirth, J. Med. Genet, 14, 309-314. 347. FinchamJ.R.S., SastryG.RK. (1974). Controlling elements in maize, Ann. Rev. Genet, 8, 15 50. 348. Flemming W. (1882). Beiträge zur Kenntnis der Zelle und ihrer Lebensscheinungen. III. Arch. Mikr. Anat, 20, 1. 349. Flemming W. (1897). Über die Chromosomenzahl beim Menschen, Anat. Anz., 14, 171. 350. Ford C.E. (1969). Mosaics and chimaeras, Br. Med. Bull, 25, 104 109. 351. Ford C. E., Hamerton J. L. (1956). The chromosomes of man, Nature, 178, 1020-1023. 352. Ford С. E., Miller O. J., Polani P.E., Almeida J. C. de, Briggs J. H. (1959). A sex-chromosome anomaly in a case of gonadal dysgenesis (Turner's syndrome), Lancet, I, 711-713. 353. Fraccaro M., Kaijser K., Lindsten J. (1959). Chromosome complement in gonadal dysgenesis (Turner's syndrome), Lancet, I, 886. 354. Fraccaro M., Kaijser K., Lindsten J. (1960). Chromosomal abnormalities in father and mongoloid child, Lancet, I, 724-727. 355. Fraccaro M., Lindsten J., Ford C. E., Iselius L. (in cooperation with many other scientists) (1980). Литература 257 The 1 lq; 22q translocation: A European collaborative analysis of 43 classes, Hum. Genet, 56, 21-51. 356. Gartler S. M., Chen S.-H. Fialkow P. J., Giblet t E. R. Singh S. (1972). X-chromosome inactivation in cells from an individual heterozygous for two X—linked genes, Nature, 236, 149. 357. Gartler S.M., Riggs A.D. (1983). Mammallian X-chromosome inactivation, Ann. Rev. Genet., 17, 155-190. 358. Gartler S. M., Sparkes R.S. (1963). The LyonBeutler hyrothesis and isochromosome X patients with the Turner Syndrome, Lancet, II, 411. 358a.G«5sfer E. (1984). Movable DNA elements and evolution. In: Geissler E., Scheler W. (eds.), Darwin today. VIII. Kuhlungsborner Kolloquium, Akademie-Verlag, Berlin. 359. German J., Archibald R., Bloom D. (1965). Chromosomal breakage in a rare and probably genetically determined syndrome of man, Science, 148, 506. 360. Giles R. E., Blanc H., Cam H. M., Wallace D. L. (1980). Maternal inheritance of human mitochondrial DNA, Proc. Natl. Acad. Sei. USA, 77, 6715-6719. 361. GitschierJ., Wood W.I., GoralkaT.M., Won K.L., Chen E. Y, Eaton D.H., Vehar G.A., Capon D.J., Lawn R.M. (1984). Characterization of the human factor VIII gene, Nature, 312, 326-330. 362. Gitschier J., Wood W. L, Tuddenham E.G.D., Shuman Μ. Α., Goralka T. M., Chen E. Y., Lawn R.M. (1985). Detection and sequence of mutations in the factor VIII gene of haemophiliacs, Nature, 315, 427-430. 363. Goodpasture C., Bloom S. E. (I975). Visualization of nuclear organizer regions in mammalian chromosomes using silver staining, Chromosoma, 53, 37-50. 364. Gray J. W., Langlois R. G., Canano A. V., Burkhart-Schulte K., Van Dilla U.A. (1979). High resolution chromosome analysis: One and two parameter flow cytometry, Chromosoma, 73, 9-27. 365. Green U.M. (1980). Transposable elements in Drosophila and other diptera, Ann. Rev. Genet, 14, 109-120. 366. Grossman L., Moldave К. (1980). Methods in Enzymology, Vol. 65, Part I, Nucleic Acids, Academic Press, New York. 367. Grouchy J. de, Lamy M., Thieffry S., Arthuis M., Salmon C. (1963). Dysmorphie complexe avec oligophrenie. Deletion des bras courts d'un chromosome 17-18, CR Acd. Sei. (Paris), 256, 1028-1029. 368. Grüneberg H. (1966). The case for somatic crossing over in the mouse, Genet Res., 7, 58-75. 369. Gusella J. F., Wexler N. S., Coneally P. M., NylerS.L., Anderson M. A., Tanzi R.E., Watkins P.C., Ottina K., Wallace U.R., Sakaguchi A. Y, Young А. В., Shoulson I., Bonilla E., Martin J.B. (1983). A polymorphic DNA marker genetically linked to Huntington's disease, Nature, 306, 234-238.
370. Habedank M., Rodewald A. (1982). Moderate Down's syndrome in three siblings having partial Trisomy 21q22.2 and therefore no SOD-I excess. Hum. Genet, 60, 74-77. 371. Hagemeijer A., Smith E.M.E. (1977). Partial trisomy 21. Further evidence taat trisomy of band 21q22 is essential for Down's phenotype, Hum. Genet, 38, 15-23. 372. Haldane J.B.S. (1936). A search for incomplete sex linkage in man, Ann. Eugen, 7, 28 57. 373. Hamerton J.L. (1968). Robertsonian translocation in man, Evidence for prezygotic selection, Cytogenetics, 7, 260-276. 374. Hamerton J.L., Ray M., Abbot J., Williamson C., Durcasse G. C. (1972). Chromosome studies in a neonatal population, Can. Med. Assoc. J., 106, 776-779. 375. Hanauer A., Levin M., Heilig R., Daegelen D., Kahn A., Mandel 3.L. (1983). Isolation and characterization of DNA clones for human skeletal muscle alpha-actin, Nucleic Acid Res., 11, 3503-3516. 376. Harnden D. G., Lindsten J.E., Buckton K., Klinger H. P. (1981). An international system for human cytogenetic nomenclature. High resolution Banding, Birth Defects: Original Article Series, Vol. XVII, No. 5. 377. Harper M.E. Ullrich A., Sounders G.F. (1981). Localization of the human insulin gene to the distal end of the short arm of chromosome 11, Proc. Natl. Acad. Sei. USA, 78, 4458-4460. 378. Hecht F., Jacky P.B., Sutherland G. R. (1982). The fragile X chromosome, Amer J. Hum. Genet, 11, 489-495. 379. Heberer G. (1940). Die Chromosomenverhältnisse des Menschen. In: Just G. (ed.), Handbuch der Erbbiologie des Menschen, Vol. I, pp. 2-30, Springer, Berlin. 380. Heitz E. (1928). Das Heterochromatm der Mouse. I. Pringsheims Jb wiss Botanik, 69, 762-818. 381. Hindley J. (1983). DNA sequencing. In: Work T. S., Bürden R. H. (eds.), Laboratory techniques in biochemistry and molecular biology, Eisevier, Amsterdam, New York, Oxford. 382. Hoo J. J., Förster C., Kindermann L, Zabel В., Hansen S. (1974). Supernumerary small ring chromosome, Human Genet, 25, 17-28. 383. Hooft C., Coetsier H., Oyre E. (1968). Syndrome de Turner et inversion pencentnque probable du chromosome 2, 45, X, 2. (p-K qt), Ann. Genet. 11, 181 183. 384. Hsu T.C. (1952). Mammalian chromosomes in vitro. I. The karyotype of man, J. Hered., 43, 167. 385. Hsu T.S. (1975). A possible function of constitutive heterochromatin: The bodyguard hypothesis, Genetics (Suppl.), 79, 137-150. 386. Hsu T.C., Pomerat C.M. (1953). Mammalian chromosomes in vitro. II. A method for spreading the chromosomes of cells in tissue culture, J. Hered., 44, 23-29. 387. Hultén M., Lindsten J. (1973). Cytogenetic aspects of human male meiosis, Adv. Hum. Genet, 4, 327-387. 9 786 Литература 388. Humphries S. E., Whittall R., Minty Α., Buckingham M., Williamson R. (1981). There are approximately 20 actin genes in the human genome, Nucleic Acid Res., 9, 4895-4908. 389. Iselius L., Lindsten J., Aurias A., Fraccaro M., and many other authors (1983). The llq; 22q translocation: A collaborative study of 20 new cases and analysis of 110 families, Hum. Genet, 64, 343-355. 390. Itakura K. (1985). Antisense RNA sequences, First Intern. Symp. on the Role of Recombinant DNA in Genetics (R. L. Teplitz et al., eds.), Crete (In the Press, 1986). 390a..JacobsP.A. (1977). Human chromosome heteromorphism (variants), Progress in Med. Genet..NS, Vol. II, 251-274. 391. Jacob F., Brenner A., Cuzin F. (1963). On the regulation of DNA replication, Cold Spring Harbor Symp. Quant. Biol., 28, 329-348. 392. Jacobs P. A. (1977). Human chromosome heteromorphism (variants), Progr. in Med. Genet (New series), 2, 251-274. 393. Jacobs P. A., Baikie A.G., MacGregor T.N., Harnden D.G. (1959). Evidence for the existence of the human "superfemale", Lancet, Π, 423-425. 394. Jacobs P.A., Brunton M., Melville U.U., Brittain R.P., McClermont W.F. (1965). Aggressive behavior, mental subnormality and the XYY male, Nature, 208, 1351-1352. 395. Jacobs P.A., Strong J.A. (1959). A case of human intersexuality having a possible XXY sexdetermining mechanism, Nature, 182, 302-303. 396. Jacobsen P., Mikkelsen M., RosleffF. (1974). The trisomy 8 syndrome: Report of two further casses, Ann. Genet (Paris), 17, 87-94. 397. Jalbert P., Sele B. (1979). Factors predisposing to adjacent-2 and 3: I disjunctions: Study of 161 human reciprocal translocations, J. Med., Genet, 16, 467-478. 398. Jeffreys A.J., Wilson V., Ihein S.L. (1985). Hypervariable "minisatellite" regions in human DNA, Nature, 314, 67-73. 399. Johamisson R., Gropp A., Winking H., Coerdt W., Rehder H., Schwinger E. (1983). Down's syndrome in the male. Reproductive pathology and meiotic studies, Hum. Genet, 63, 132-138. Дата добавления: 2015-12-16 | Просмотры: 536 | Нарушение авторских прав |