АкушерствоАнатомияАнестезиологияВакцинопрофилактикаВалеологияВетеринарияГигиенаЗаболеванияИммунологияКардиологияНеврологияНефрологияОнкологияОториноларингологияОфтальмологияПаразитологияПедиатрияПервая помощьПсихиатрияПульмонологияРеанимацияРевматологияСтоматологияТерапияТоксикологияТравматологияУрологияФармакологияФармацевтикаФизиотерапияФтизиатрияХирургияЭндокринологияЭпидемиология
|
Приложение 8. 239 4 страница
400. Jones R.C., Potter S.S. (1985). LI sequences in HeLa extrachromosomal circular DNA: Evidence for circularization bu homologous recombination, Proc. Nat. Acad. Sei. USA, 82, 1989-1993.
401. Joseph J.L., BraschJ.M., Smyth D.R. (1982). Pattern of exchange induced by mitomycin С in C-bands of human chromosomes. II. High frequency of Y-Y exchange in XYY cells, Hum. Genet., 62, 246-348.
4Q\n.Kaiser P. (1984). Pericentric inversions. Problems and significance for clinical genetics, Hum. Genet, 68, 1-47.
402. Kakati S., N thill M., Sinah A. (1973). An attempt to establish trisomy 8 syndrome, Hum. Genet, 19, 293-300.
403. Khalili K., Salas С., Weinemann P. (1983). Isolation and characterization of human actin
genes in phage Lambda vectors, Gene, 21, 9-17.
404. Kirsch-Volders M., Hens L., Susanne C. (1980). Telomere and centremere association tendencies in the human male metaphase complement, Hum. Genet, 54, 69-74.
405. Kjessler B. (1966). Karyotype, meiosis and spermatpgenesis in a sample of men attending an infertility clinic, Monogr. Hum. Genet. 2 Karger, Basel.
406. Koske-Westphal Th., Passarge E. (1974). Die Chromosomen des Menschen und ihre Untersuchung in somalischen Zellen. In: Vogel. F. (ed.), Handbuch der allgemeinen Pathologie, Vol. IX, Erbgefüge, pp. 261-323, Springer, Berlin, Heidelberg, New York.
407. Koskull H., von, Aula P. (1974). Inherited (13, 14) translocation and reproduction, Hum. Genet, 24, 85-91.
408. Ките J., Tolksdorf M., Wiedemann H.-R. (1975). Cat eye syndrome, Hum. Genet, 26, 271-289.
409. Kurilo L.F. (1981). Oogenesis in antenatal development in man, Hum. Genet, 57, 86-92.
410. KurnitD.M. (1979). Satellite DNA and heterochromatin variants: The case for unequal mitotic crossing over, Hum. Genet, 47, 169-186.
411. Latt S.A. (1973). Microfluorometric detection of deoxyribonucleic acid replication in human metaphase chromosomes, Proc. Natl. Acad. Sei. USA, 70, 3395-3399.
412. Latt S. A., Schreck R R., Laveday K. S., Dougherty C.P., Schuller С. С. F. (1980). Sister chromatid exchanges, Adv. in Hum. Genet, 10, 267-331.
413. Lauritsen J.G. (1977). Genetic aspects of spontaneous abortion, University of Aarhus, Laegeforeninges.
414. Lauritsen J. G., Bolund L., Friedrich U., Therkelsen A.L. (1979). Origin of triploidy in spontaneous abortuses, Ann. Hum. Genet, 43, 1-6.
415. Lejeune J. (1968). De la duplication de structures circulaires, Ann. Genet (Paris), 11, 71-77.
416. Lejeune J., Berger R. (1965). Sur deux observations familiales de translocations complexex, Ann. Genet. (Paris), 8, 21-30.
417. Lejeune J., Gautier M., TurpinM.R. (1959). Etude des chromosomes somatiques de neuf enfants mongoliens, CR Acad. Sei. (Paris), 248, 1721-1722.
418. Lejeune J., Lafourcade J., Berger R., VialatteJ., Roeswillwald M., Seringe P., Turpin R. (1963). Trois cas de deletion partielle du bras court d'un chromosome 5, CR Acad. Sei. (Paris), 257, 3098-3102.
419. Léonard C., Hazael-Massieux P., Bocquet L., Larget-Piet L., Boue J. (1975). Inversion péricentrique inv. (2) (pllql3) dans les familes non apparenlées, Hum. Genêt, 28, 121-128.
420. LifschitzE., LindsleyD.L. (1972). The role of X-chromosome inactivation during spermatogenesis, Proc. Natl. Acal. Sei. USA, 69, 182-186.
421. LilleyD.M.J., Pardon J. F. (1979). Structure
Литература 259
and function of chromatin, Ann. Rev. Genet., 13, 197-233.
422. Lubs Η. Α., Ruddle F. H. (1970). Applications of quantitative karyotypy to chromosome variantion in 4400 consecutive newborns. In: Jacobs P. A., Price W.H., L aw P. (eds.), Human population cytogenetics, pp. 120-142, Pfizer Medical Monographs 5, University of Edinburgh Press, Edinburgh.
423. LyonM.F. (1971). Possible mechanisms of Y chromosome inactivation, Nature, New Biol., 232, 229.
424. LyonM.H. (1968). Chromosomal and subchromosomal inactivation, Ann. Rev. Genet, 2, 31-52.
425. Lyon M. F. (1961). Gene action in the X-chromosome of the mouse, Nature, 190, 372-373.
426. Lyon M. F. (1961). Gene action in the X-chromosome of mammals including man, Proceedings 2nd International Conference of Human Genetics, Rome, August 1961, pp. 1228-1229.
427. Madan K. (1983). Balanced structural changes involving the human X: Effect on sexual phenotype, Hum. Genet, 63, 216-221.
428. Maddox J. (1984). Who will clone a chromosome? Nature, 312, 306.
429. Mager D.L., Henthom P.S. (1984). Identification of a retroviruslike repetitive element in human DNA, Proc. Natl. Acad. Sei. UCA, 81, 7510-7514.
430. Martin G.M. (1978). The pathobiology of aging, University of Washington Medicine, 5, 3-10.
431. Martin R.H., Balkan W., Burns K., LinC.C. (1982). Direct chromosomal analysis of human spermatozoa, Amer. J. Hum. Genet, 34,459-468.
432. Martin R. H., Balkan W., Bums K., RademakerA.W., LinC.C., RuddN.L. (1983). The chromosome constitution of 1000 human spermatozoa, Hum. Genet, 63, 305-309.
433. McClintock B. (1956). Controlling elements and the gene, Cold Spring Harbor Symp. Quant. Biol., 21, 197-144.
434. Merril C. R., Harrington M. G. (1985). The search for mitochondrial inheritance of human diseases, TIG, 1, 140-144.
435. Metz С. W. (1916). Chromosome studies on the diptera. II. The paired association of the chromosomes in the diptera and its significance, J. Exp. Zool., 21, 213.
436. Mikelsaar A.-V., Schmid M., Krone W., Schwarzacher H.G., Schnedl W. (1977). Frequency of Ag-stained nucleolus organizer regions in the acrocentric chromosomes of man, Hum. Genet, 31, 13-17.
437. Miklos G. L. G., John B. (1979). Heterochromatin and satellite DNA in man: properties and prospects, Amer. J. Hum. Genet, 31, 264-280.
439. Miller O. J. (1985). Dosage compensation in mammals: Why does a gene on the inactive X uield less product than one on the active X? Hum. Genet, 69, 97-101.
440. Miller O.L., Beatty B.R. (1969). Visualization of molecular genes, Science, 164, 955-957.
441. Miller O.L., Miller D. A., Warburton D. (1973).
Application of the new staining techniques to the study of human chromosomes, Prog. Med. Genet, 9, 1-48.
442. Miller O.L., Schreck R.R., Beiser S.M., Erlanger B. F. (1973). Immunofluorescent studies of chromosome banding with antinucleotide antibodies. In: Nobel Symposium 23: Chromosome identification, pp. 43-48, Academic Press, New York, London.
443. Mikkelsen M. (1971). Down's syndrome. Current stage of cytogenetic research, Hum. Genet, 12, 1-28.
444. Mikkelsen M., Hansson A., Jacobsen P., Hobolth N. (1975). Tranclocation (13q21q). Four generation family study with analysis of satellite associations, fluorescent markers, and prenatal diagnosis, Hum. Genet, 27, 303-307.
445. Mikkelsen M., Stene J. (1970). Genetic counseling in Down's syndrome, Hum. Hered-, 20, 457-464.
446. Milunsky A. (1973). The prenatal diagnosis of hereditary disorders, Thomas, Springfield.
447. MoorheadP.S., Nowell P.C., MellmanW.J., BattipsD.M., Hungerford D. A. (1960). Chromosome preparations of leukocytes cultured from human peripheral blood, Exp. Cell Res., 20, 613-616.
448. Morgan Т.Н. (1910). Sex-limited inheritance in drosophila, Science, 32, 120-122.
449. Morton N. E., Jacobs P. A., Frackiewicz A. (1975). The effect of structural aberrations of the chromosomes on reproductive fitness in man. I. Metoodology, Clin. Genet, 8, 159-168.
450. Morton N. E., Lindsten J., Iselius L., Yee S. (1982). Data and theory for a revised chiasma map of man, Hum. Genet, 62, 266-270.
451. Moser H., Emery A.E.H. (1974). The manifesting carrier in Duchenne muscular dystrophy, Clin. Genet, 5, 271-284.
453. Muller H.J. (1941). Induced mutations in drosophila. In: Genes and chromosomes, structure and organization, Cold. Spring. Harbor Symp. on Quant Biol., Vol. ГХ, 151-167.
454. Mullinger A.M., Johnson R. T. (1980). Packing DNA into chromosomes, J. Cell Sei., 46, 61-86.
455. Nagakome Y., Hmura K., Tangiuchi K. (1973). Points of exchange in a human no. 5 ring chromosome, Cytogenet Cell Genet, 12, 35-39.
456. Natarajan A. T., Zwanenburg T.S.B. (1982). Mechanismsfor chromosomal aberrations in mammalian cells, Mulation Research, 95, 1-6.
457. Nathans D. (1980). Restriction endonucleases, Simian Virus 40, and the new genetics, Science, 206, 903-909.
458. Niebuhr E. (1974). Triploidy in man, Hum. Genet, 21, 103-125.
459. Niebuhr E. (1972). Localization of the deleted segment in the cri-du-caat syndrome, Hum. Genet., 16, 357-358.
460. Noel В., Quack В., Rethoré M. О. (1976). Partial deletions and trisomies of chromosome 13; mapping of bands associated with particular malformations, Clin. Genet, 9, 593-602.
Литература
461. Nowakowski H., Lenz W., Parada J. (1958). Diskrepanz zwischen Chromatinbefund und chromosomalem Genschlecht beim KlinefelterSyndrom. Klin. Wochenschr., 36, 683-684.
462. Nowakowski H., Lenz W., Parada J. (1959). Diskrepanz zwischen Chromatinbefund und genetischem Geschlecht beim Klinefelter-Syndrom, Acta Endocrinol, 30, 296 320.
463. OhnoS., Kaplan W. D., Kinosita R. (1959). Formation of the sex chromatin by a single X chromosome in liver cells of Rattus norvegicus, Exp. Cell Res., 18, 415-418.
464. Ohno S., Makino S. (1961). The single-X nature sex chromatin in man, Lancet, I, 78-79.
465. 0ster J., Mikkelsen M., Nielsen A. (1964). The mortality and causes of death in patients with Down's syndrome (mongolism), International Copenhagen Congress of Scientific Study of Mental Retardation, 1, 231.
466. Fachmann U., Rigler R. (1972). Quantum yield of acridities interacting with DNA of defined basesequence, Exp. Cell Res., 72, 602.
467. Painter T.S. (1923). Studies in mammalian spermatogenesis. II. The spermatogenesis of man, J. Exp. Zool., 37, 291-321.
468. Paris Conference 1971: Standartization in human cytogenetics, Cytogenetics, 11, 313-362 (1972).
469. Passarge E. (1979). Emil Heitz and the concept of heterochromatin: Longitudinal chromosome differentiation was recognized fifty years ago, Am. J. Hum. Genet., 31, 106-115.
470. Passarge E., Fries E. (1973). X-chromosome inactivation in X-linked hypohidrotic ectodermal dysplasia, Nature New Biology, 245, 58-59.
471. Patau K. (1960). The identification of individual chromosomes, especially in man, Am. J. Hum. Genet., 12, 250-276.
472. Patau K., Smith D. W, Therman E., Inhorn S.L., Wagner H. P. (1960). Multiple congenital anomaly caused by an extra chromosome, Lancet, I, 790-793.
473. Pawlowitzki I. H. (1972). Frequency of chromosome abnormalities in abortions, Hum. Genet. 16, 131-136.
474. Pearson P. L., Bobrow M., (1970). Fluorescent staining of the Y chromosome in meiotic stages of the human male, J. Reprod. Fertil., 22, 177-179.
475. Penrose L.S., Delhanty J.D.A. (1961). Triploid cell cultures from a macerated foetus, Lancet, I, 1261.
476. Pirastu M. (1985). The oligonucleotide technique for antenatal diagnosis of ß-Thalassemia in Italy. In: Teplitz R. L. et al. (eds.) First Intern. Symp. on the Role of Recombinant DNA in Genetics Crete (In the press 1986).
477. Polani P.E. (1962). Sex chromosome abnormalies in man. In: Hamerton J. L. (ed.), Chromosomes in medicine, pp. 73 139, Heinemann, London.
478. Polani P. E., Bishop P. M. F., lennox В., Ferguson-Smith U.A., Stewart J.S.S., Plader A. (1958). Color vision studies in the X-chromosome
constitution of patients with Klinefelter's syndrome, Nature, 182, 1092-1093.
479. Polani B. E., Briggs J. H., Ford С. Е., Clarke С. М., BergJ.M. (1960). A mongol child with 46 chromosomes, Lancet, I, 721-724.
480. Ouie P.O., White J.G., Holmes В., Good R.A. (1967). In vivo bactericidal capacity of human polymorphonuclear leucocytes: Diminished activity in chronic granulomatous disease of childhood, J. Clin. Invest, 46, 668-679.
481. RaoP.N., Johnson R. T., Sperling К. (1982). Premature chromosome condensation, Application in basic, clinical and mutation research, Academic Press, New York etc.
482. RappoldG.A., Vosberg H.-P. (1984). Chromosomal localization of a human myosin heavy-chain gene by in situ hybridization, Hum. Genet, 65, 195-197.
483. Richards B. W. (1969). Mosaic mongolism, J. Ment. Défie. Res., 13, 66-83.
484. Rigler R. (1966). Microfluoreometric characterization of intracellular nucleic acids and nucleoproteins by acridine orange, Acta Physiol. Scand., 67, [Suppl. 267], 1, 485, Röhme D., Heneen W. K. (1982). Banding patterns in prematurely condensed chromosomes and the underlying structure of the chromosomes, pp. 131-157, In: Rao P. N., Johnson R. T., Sperling K., (eds.), Premature chromosome condensation, Academic Press, New York etc.
486. Ropers H. H., Migl B., Zimmer J., Muller С. R. (l 981 a). Steroid sulfatase activity in cultured fibroblasts of XX males, Cytogenet. Cell Genet, 30, 168-173.
487. Ropers H. H., Migl B., Zimmer J., Fraccaro M., Maraschio P.P., Westerfeld A. (1981b). Activity of steroid sulfatase in fibroblasts with numerical and structural X chromosome aberrations, Hum. Genet, 57, 345-356.
488. Ropers H.H., Wienker T.F., Grimm T., Schroetter K., Bender K. (1977). Evidence for preferential X-chromosome inactivation in a family with Fabry disease, Am. J. Hum. Gen., 29, 361-370.
488a.Äo«yer F., Simmler M. С., Johnsson С., VergnatidG., Cooke H.J., Weissenbach J. (1986). A gradient of sex linkage in the pseudoautosomal region of the human sex chromosomes, Nature, 319, 291-295.
489. RudokE., Jacobs P.A., Yanaginachi R. (1978). Direct analysis of the chromosome constitution of human spermatozoa, Nature, 274, 911-913.
490. Ruzicka F. (1973). Über die Ultrastruktur menschlicher Metaphase-Chromosomen, Hum. Genet, 17, 137-144.
491. Sachs L. (1953/54). Sex-linkage and the sex chromosome in man, Ann. Hum. Genet., 18, 255-261.
492. Southern E.M. (1975). Detection of specific sequences among DNA fragments separated by gel electrophoresis, J. Mol. BioL, 98, 503-517.
493. Setlow J.K., Hollaender A. (1979). Genetic engineering: Principles and methods, Vol. 1, Plenum Press, New York.
494. Shmookler Reis R.J., Lumpkin C.K., McGill J. R., Riabowol К. Т., Goldstein S. (1983). Extrachro-
Литература 261
mosomal circular copies of an "inter-Alu" unstable sequence in human DNA are amplified during in vitro and in vivo ageing, Nature, 301, 394-398.
495. Smith D. W., Patau K., Therman E., tnhorn S. L. (1960). A new autosomal trisomy syndrome: Multiple congenital anomalies caused by an extra chromosome, J. Pediatr., 57, 338-345.
496. Smith H. O. (1979). Nucleotide sequence specificity of restriction endonucleases, Science, 205, 455-462.
497. Solari A. J. (1980). Synaptonemal complexes and associated structures in microspread spermatocytes, Chromosome, 81, 315-337.
498. Sperling K. (1984). Frequency and origin of chromosome abnormalities in man. In: Obe B. (ed.), Mutation in man, pp. 128-146, Spinger, Berlin, Heidelberg, New York.
449. Sperling K. (1984). Genetische Sektion-Anatomie der menschlichen Gene. In: (Passarge E., ed.), pp. 73-100, Verlag Chemie, Darmstadt.
500. Sperling K., Rao P. N. (1974). The phenomenon of premature chromosome condensation: Its relevance to basic and applied research, Humangenetik, 23, 235-258.
501. Summitt R.L., Martens P.R., Wuroy R.S. (1973). X-autosome translocation in normal mother and effectively 21-monosomic daughter, J. Pediatr., 84, 539-546.
50\a.Schaefer M.S.D. (1983). Segregation and Pathologie autosomaler familiärer Translokationen bein Menschen, Diss. Univ. Kaiserslautern.
502. Schemp W., Meer B. (1983). Cytologie evidence for three human X-chromosomal segments escaping inactivation, Hum. Genet, 63, 171-174.
503. Schinzel A. (1979). Autosomale Chromosomenaberrationen, Archiv, für Genetik, 52, 1-204.
504. Schleiermacher E., Schliebitz U., Steffens C. (1974). Brother and sister with trisomy Юр: А new syndrome, Hum. Genet., 23, 163-172.
505. Schmid С. W., Jelinek W. R. (1982). The Alu family of dispersed repititive sequences, Science, 216, 1065-1070.
506. Schmidt E. R. (1985). Sequenzen von DNA. In: Blin N., Trendelenburg M. F., Schmidt E. R. (eds.), Molekular- und Zellbiologie, pp. 35-51, Springer Verlag, Berlin, Heidelberg, New York.
507. Schmidtke J., Cooper D. N. (1983). A list of cloned DNA sequences, Hum. Genet., 65, 19-26.
508. Schmidtke J., Cooper D. N. (1984). A list of cloned human DNA sequences-Supplement, Hum. Genet., 67, 111-114.
509. Schmidtke J., Epplen J. T. (1980). Sequence organization of animal nuclear DNA, Hum. Genet, 55, 1-18.
510. Schnedl W. (1971). Banding pattern of human chromosomes, Nature, 233, 93.
511. Schnedl W. (1978). Structure and variability of human chromosomes analysed by recent techniques, Hum. Genet., 41, 1-10.
512. Schnedl W. (1974). Banding patterns in human chromosomes visualized by Giemsa staining after various pretreatments. In: Schwarzacher H. G., Wolf U. (eds.), Methods in human
cytogenetics, pp. 95-116, Springer, New York, Heidelberg, Berlin.
513. Schneider E.L., Epstein C.J. (1972). Replication rate and life span of cultured fibroblasts in Down's syndrome, Proc. Soc. Exp. Biol. Med., 141, 1092-1094.
514. Schneiderman L.J., Smith C.A.B. (1962). Nonrandom distribution of certain homologous pairs of normal human chromosomes in metaphase, Nature, 195, 1229-1230.
515. Schroeder T.M., Anschütz F., Knopp A. (1964). Spontane Chromosomenaberrationen bie familiärer Panmyelopathie, Hum. Genet, 1, 194-196.
516. Schwarzacher H. G. (1974). Fluorescence microscopy of chromosomes and interphase nuclei. In: Schwarzacher H. G., Wolf U. (eds.), Methods in human cytogenetics, pp. 83-93, Springer, New York, Heidelberg, Berlin.
517. Schwarzacher H.G. (1970). Die Ergebnisse elektronenmikroskopischer Untersuchungen an somatischen Chromosomen des Menschen, Hum. Genet, 10, 195-208.
518. Schwarzacher H. G., Wachtier F. (1983). Nucleolus organizer regions and nucleoli, Hum. Genet, 63, 89-99.
519. Simpson J.L., (1976). Disorders of sexual differentiation, Etioloqy and clinical delineation, Academic Press, New York.
520. Starlinger P. (1980). IS elements and transposons, Plasmid, 3, 241-259.
521. Stern C. (1936). Somatic crossing-over and segregation in Drosophila melanogaster, Genetics, 21, 625-730.
522. Stern C. (1959). The chromosomes of man, J. Med. Educ., 34, 301-314.
523. Strayer D., Heintz N.. Roeder R., Gillespie D. (1983). Three organisations of human DNA, Proc. Nat. Acad. Sei. USA, 80, 4770-4774.
524. Taylor A. L. (1963). Bacteriophage-induced mutation in Eschericha coli, Proc. Natl. Acad. Sei. USA, 50, 1043-1051.
525. Taylor J.H. (I960). Asynchronous duplication of chromosomes in cultured cells of Chinese hamster, J. Biophys. Biochem. Cytolog., 7, 455-464.
526. Taylor K. M., Wolfinger H. L., Brown M.-G., Chadwick D.L (1975). Origin of a small metacentric chromosome. Familial and cytogenetic evidence, Clin. Genet, 8, 364-369.
527. Teplitz R. L. (1985). The use of synthetic oligonucleotides in and prenatal diagnosis of genetic disease. In; Teplitz R. L. et al. (eds.), First Intern. Symp. on the Role of Recombinant DNA in Genetics, Crete (In the press, 1986).
528. Therman £., Meyer-Kuhn E. (1981). Mitotic crossing-over and segregation in man, Hum. Genet, 59, 93-100.
529. Therman E., Patau K. (1974). Abnormal X chromosomes in man. Origin behavior and effects, Hum. Genet, 25, 1-16.
530. Therman E., Sarto G. E., Palmer C. G., Kallio H., Dennis ton C. (1979). Position of the human X inactivation center on Xp., Hum. Genet, 50, 59-64.
531. Tode J.J., Knopf J. L., Wozney J.M., Sutz-
Литература
man L. Α., Bueker J.L., Pittman D.D., Kaufman R.}., Brown E., Shoemaker Ch., Orr E. C., Amphlett G. W., Foster W. В., Сое M. L., Knutson G. 3., Pass D. N. Hewick R. M. (1984). Molecular cloning of a cDNA encoding human antihaemophilic factor, Nature, 312, 342-347.
532. TJio H.J., Levan A. (1956). The chromosome numbers of man, Hereditas, 42, 1-6.
533. 7//0 H. J., Puck T. T. (1958). The somatic chromosomes of man, Proc. Natl. Acad. Sei. USA, 44, 1229-1237.
535. Trendelenburg M. F. (1983). Progress in visualization of eukaryotic gene transcription, Hum. Genet., 63, 197-215.
536. Vehar G. A., Keyt В., Eaton D., Rodriguez H., O'BrianD.P., Rotblat P., Oppermann H., KeckR., WoodW.l., Harkins R.N., Tuddenham E.G.D., Lawn R.M., Capon D.J. (1984). Structure of human factor VIII, Nature, 312, 337-342.
537. Waardenburg P. J. (1932). Das menschliche Auge und seine Erbanlagen, Bibliogr. Genet., 7.
538. Wachtel S. (ed.), Errors of sex determination (Proc. of the Kroc. Foundation Conf.), Hum. Genet., 58, 1-127.
539. Wallace R.B. (1985). The use of synthetic DNA hybridization probes as tools for genetic analysis. In: Teplitz R. L. et al. (eds.), First Intern. Symp. on the Role of Recombinant DNA in Genetics, Crete (In the press, 1986).
540. Weisblum В., de Haseth P. L. (1972). Quinacrine, a chromosome stain specific for deoxyadenilate-de--oxy-thymidinate-rich regions of DNA, Proc. Natl. Acad. Sei. USA, 69, 629.
541. Wilson G.N. Lynne Szura L., Rushford C., Jackson D., Erickson J. (1982). Structure and variation of human ribosomal DNA: The external transcribed spacer and adjacent regions, Am. J. Hum. Genet., 34, 32-49.
542. Windhorst D. В., Holmes В., Good R. A. (1967). A newly defined X-linked trait in man with demonstration of the Lyon effect in carrier females, Lancet, I, 737-739.
543. Winiwarter H. von (1912). Etudes sur la spermatogenese humaine. I. Cellule de Sertoli. II. Hétérochromosome et mitoses de L'epithelium seminal, Arch. Biol. (Liege), 27, 91-189.
544. Wolf U., Reinwein H., Forsch R., Schroter R., Baitsch H. (1965). Defizienz an den kurzen Armen eines Chromosoms Nr. 4, Hum. Genet., l, 397-413.
545. Wolff E. de, Scharer K., Lejeune J. (1962). Contribution a l'étude des jumeaux mongoliens. Un cas monozygotréme heterocaryote, Nelv. Paediatr. Acta, 17, 301-328.
546. Wood W.I., Capon D.J., Simonsen C.C., Eaton D.L., Gïtschier J., Keyt B., Seeburg P. H., Smith D. H., Hollingshead P., Wion K. L., Delwart E., Tuddenham E. G. D., Vehar G. A., Lawn R. M. (1984). Expression of active human factor VIII from recombinant DNA clones, Nature, 312, 330-337.
547. Wollenberg С., Kief aber M. P., Zang K.D. (1982). Quantitative studies on the arrangement of human metaphase chromosomes VIII.
Localization of homologous chromosomes, Hum. Genet, 60, 239-248.
548. WymanA.R., White R. (1980). A highly polymorphic locus in human DNA, Proc. Natl. Acad. Sei. USA, 77, 6754-6758.
549. Yuncken C. (1968). Meiosis in the human female, Cytogenetics, 7, 234-238.
550. Yunis J.J. (1981). Mid-prophase human chromosomes. The attainment of 2000 bands, Hum. Genet., 56, 293-298.
551. Zankl H., Zang K.D. (1979). Quantitative studies on the arrange ment of human metaphase chromosomes. VII. The association pattern of acrocentric chromosomes in carriers of Robertsonian translocations and in their relatives with normal karyotypes, Hum. Genet., 52, 119-125.
Литература к главе 3 и к приложениям 1, 2, 3, 4, 5, 6, 7, 9
552. AirdL, Bentall H.H., Roberts J. A.F. (1953). A relationship between cancer of stomach and the ABO group, Br. Med. J., 1, 799-801.
553. Albert E. D., Ваш M. P., MayrW.R. (eds.). Histocompatibility Testing 1984. SpringerVerlag, Berlin, Heidelberg, New York.
554. Allen F., Amos D.B., Bathelor R., Bodmer W, Ceppelini R., Dausset J., Engelfriet C., Jeannet M., Kissmey er-Nielsen P., Morris P., Payne R., Terasaki P., vanRood J. J., Waiford R., Zmijewski C., Albert E., Mattuiz P., Mickey M.R., Piazza A. (1970). Joint report of 4th Intern Histocompatibility Workshop, Histocompatibility testing (Terasaki P., ed.), Munksgaard, Kopenhagen, 17-47.
555. Allison A. C., Blumberg B.S. (1958). Domonance and recessivity in medical genetics, Am. J. Med., 25, 933-941.
556. Amos D. В., KostyuD.D. (1980). HLA-A central immunological agency in man, Adv. in Hum. Genet, 10, 137-208.
557. Andreassen M. (1943). Haemofili i Danmark. Opera ex Domo Biologiae Hereditariae Humanae Universitatis Hafniensis Munksgaard, Vol. 6, Copenhagen.
558. Antonarakis S. E., Copeland K. L., Carpenter R. J. Jr., CartaC.A., Hoyer L.W., Coskey С. T., TooleJ.J., Kazazian H.H., Jr. (1985). Prenatal diagnosis of haemophilia A by factor VIII gene analysis, Lancet 1, 1407-1409.
559. Ball S. P., Cook P.J.L., Mars M., Buckton K.E. (1982). Linkage between dentinogenesis imperfacta and GC, Ann. Hun. Genet, 46, 35-40.
560. Baralle P.E., Shoulders C.C. (1984). Lipoprotein genes and hyperlipidemia, Schweiz. Med. Wschr., 114, 1351-1358.
561. Baieson W., Punnett R.G. (1908). Saunders: Confirmations and extensions of Mendel's principles in other animals and plants, Report to tee Evolution Committee of the Royal Society (London).
Литература 263
562. Bauer К. H. (1927). Hpmoiotransplantation von Epidermis bei einei igen Zwillingen, Beitr. Klin. Chir., 141, 442-447.
563. Becker P.E. (1964). Myopathien. In: Becker P. E. (ed.), Humangenetik, ein kurzes Handbuch, Vol. III/I, pp. 411-550, Thieme, Stuttgart.
564. Becker P. E. (1953). Dystrophia musculorum progressiva, Thieme, Stuttgart.
565. Becker P.E. (1972). Neues zur Genetik und Klassifikation der Muskeldystrophien, Hum. Genet, 17. 1-22.
S65a.Bell J. (1934). Huntington's chorea, Treasury of Human Inheritance 4.
566. Bell J. (1947). Dystrophia myotonica and allied diseases, Treasury of Human Inheritance 4 Teil V
567. Benirschke K., KimC.K. (1973). Multiple pregnancy, N. Engl. J. Med., 228, 1276-1284; 1329-1336.
568. Bennett T. (1975). The T-locus of the mouse, Cell, 6, 441-454.
569. Benzer S. (1957). The elementary units of heredity. In: McElroy W. D., Glass B. (eds.), The chemical basis of heredity, John Hopkins University Press, Baltimore, pp. 70-93.
570. Berg K. (1983). Genetics of coronary heart disease, Progr. Med. Genet, N. S., 5, 35-90.
571. Bernstein F. (1931). Zur Grundlegung der Chromosomentheorie der Vererbung beim Menschen, Z. Induktive Abstammungs - Vererbungslehre, 57, 113-138.
572. Bernstein F. (1930). Fortgesetzte Untersuchungen aus der Theorie der Blutgruppen, Z. Induktive Abstammungs-Vererbungslehre, 56, 233-237.
573. Bernstein F. (1930). Über die Erblichkeit der Blutgruppen, Z. Induktiven AbstammungsVererbungslehre, 54, 400.
574. Bernstein F. (1925). Zusammenfassende Betrachtungen über die erblichen Blutstrukturen des Menschen, Z. Induktive AbstammungsVererbungslehre, 37, 237.
575. Berwick D.M., Cretin S., Keeler E.B. (1980). Cholesterol, Children, and Heart Disease. An Analysis of Alternatives, Oxford, New York.
576. Bhende Y.M., Deshpande C. K., Bhata H.M., Sanger R., Race R.R., Morgan W.T.J., Watkins W.M. (1952). A "new" blood-group character related to the ABO system, Lancet, I, 903-904.
577. Bieber F. R., Nance W. E., Morton C. C., Brown J. A., Redwine F. O., Jordan R. L., Mohanakumar T. (1981). Genetic studies of an acardiac monster: Evidence of polar body twinning in man, Science, 213, 775-777.
578. Bilheimer D.W., Goldstein J. L., Grundy S.M., StarzlT.E., Brown M.S. (1984). Liver transplantation to provide low-density-lipoprotein receptors and low plasma cholesterol in a child with homozygous familial hypercholesterolemia, N. Engl. J. Med., 311, 1658-1664.
Дата добавления: 2015-12-16 | Просмотры: 580 | Нарушение авторских прав
|