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Приложение 8. 239 6 страница
745. Kravitz K., Skolnick M., Edwards C., Cartwright G., Amos B., Carmelli D., Baty B. (1978). Pedigree analysis of the linkage between HLA and hemochromatosis. In: Morton N. E., Chung C. S. (eds.), Genetic epidemiology, Academic Press, New York, pp. 241-246.
746. Krüger J. (1973). Zur Unterscheidung zwischen multifaktoriellen Erbgang mit Schwellenwerteffekt und einfachen diallem Erbgang, Hum. Genet., 17, 181-252.
747. Krüger J., Propping P. (1976). Rückgang der Zwillingsgeburten in Deutschland, Dtsch. Med. Wochenschr., 101, 475-480.
748. Kruger J., Vogel F. (1975). Population genetics of unequal cros sing over, J. Mol. Evol, 4, 201—247
749. Kueppers F. (1975). сц-Antitrypsin. In: Becker P. E. (ed.), Humangenetik, ein kurzes Handbuch, Vol. 1/3, Thieme, Stuttgart, pp. 35-49.
750. Kunkel L. M., Tantravahi U., Eisenhard M., Latt S. (1978). Regional localization on the human X of DNA segments cloned from flow sorted chromosomes, Nucleic Acid Res., 10, 1557-1578.
751. Kurachi K., Chandra T., Degen S. J., White T. T., Marchioro T.L., Woo S. L. С., Davie E. W., (1981). Cloning and sequence of cDNA coding for alpha-antitrypsin, Proc. Natl. Acad. Sei. USA, 78, 6826-6830.
752. Lalouel J. M., Morton N. E., MacLean C. J., Jackson J. (1977). Recurrence risk in complex inheritance with special regard to pyloric stenosis, J. Med. Genet., 14, 408-414.
753. Landsteiner K., Wiener A.S. (1940). An agglutinable factor in human blood recognized by immune sera for rhesus blood, Proc. Soc. Exp. Biol. Med., 43, 223.
754. Lange К., Boehnke M. (1982). How many polymorphic genes will it take to span the
Литература 269
human genome? Amer. J. Hum. Genet., 34, 842-845.
754a. Lange K., Page B. M., Eiston R. С. (1975). Age trends in human hiasma frequencies and recombination fractions. I. Chiasma frequencies, Am. J. Hum. Genet, 27, 410-418.
755. Laurell C.-B., Eriksson S. (1963). The electrophoretic at- globulin pattern of serum 04antitrypsin deficiency, Scand. J. Clin. Lab. Invest., 15, 132.
756. Lemser H. (1938). Zur Erb- und Rassenpathologie des Diabetes mellitus, Arch. Rassenbiol., 32, 481.
757. Lenz F. (1923). Ubersterblichkeit der Knaben im Lichte der Erbhchkcitslehre, Arch. Hyg., 93, 126-150.
757a. Lenmark A. (1985). Molecular biology of type 1 (insulin-dependent) diabetes mellitus, Diabetes, 28, 195-203.
758. Lenz W. (1959). Ursachen des gesteigerten Wachstums der heutigen Jugend. In: Akzeleration und Ernährung Fettlösliche Wirkstoffe, Vol. 4.
759. Lenz W. (1961). Zur Genetik der Incontinentia pigmenti, Ann. Paediatr. (Basel), 196, 141.
760. Lenz W. (1975). Half chromatid mutations may explain incontinentia pigmenti in males, Am. J. Hum. Genet, 27, 690-691.
761. Lenz W. (1973). Vererbung und Umwelt bie der Entstehung von Missbildungen, Uumanbiologie, 121, 132-145.
762. Levine P., Stetson R. E. (1939). An unusual case of intragroup agglutination, J. Am. Med. Assoc., 113, 126-127.
763. Levy R. I. (1981). Declining mortality in coronary heart disease, Arteriosclerosis, 1, 312-325.
764. Lewis E. B. (1951). Pseudoallelism and gene evolution, Cold Spring Harbor Symp. Quant. Biol., 16, 159-174.
765. Lieberman R., Humphrey W., (1972). Association of the H-2 type with genetic control of immune responsiveness to (y2a) allotypes in the mouse, J. Exp. Med., 136, 1222-1230.
766. Lilly F. (1966). The inheritance of susceptibility to the Gross leukemia virus in mice, Genetics, 53, 529-539.
767. Lundsgaard R. (1944). Leber's disease. A généalogie, genetic and clinical study of 101 cases of retrobulbar optic neuritis in 20 Danish families, Acta Ophthalmol. /Suppl/ (Kbh.), 30.
768. Luxemburger H. (1935). Untersuchungen an schizophrenen Zwillingen und ihren Geschwistern zur Prüfung der Realität von Manifestationsschwankungen, Z. Gesamte Neurol. Psychiat, 154, 351-394.
769. Luxenburger H. (1940). Zwillingsforschung als Methode der Erbforschung beim Menschen. In: Just G., Bauer K. H., Hanhart E., Lange J. (eds.), Handbuch der Erbbiologie des Menschen, Vol. II, Methodik, Genetik der Gesamtperson, Springer, Berlin, pp. 213-248.
770. Maartmenn-Moe K., Magnus P., Golden W., Berg K. (1981). Genetics of the low density
lipoprotein receptor: III. Evidence for multiple normal alleles at the low density lipoprotein receptor locus, Clin. Genet., 20, 113-129.
771. Maartmann-Moe K., Magnus P., Borresen A.-L., Berg K. (1981). Low density lipoprotein receptor activity in cultured fibroblasts from subjects with or without ischémie heart disease (in the ab sence of familial hypercholesterolemia), Clin. Genet, 20, 337-346.
772. Madiener M. (1928). Eine Bluterfamilie, Arch. Rassenbiol., 20, 390-394.
773. Mann J. D., Cahan A., Gelb A., Fischer N., Hamper J., Tipett P., Sanger R., Race R.R. (1962). A sex-linked blood group, Lancet, I, 8.
774. Maroteaux P. (1974). Les maladies esseuses de l'enfant, Flammarion, Paris.
775. Marsh D.G., Meyers D.Α., Bias W.B. (1981). The epidemiology and genetics of atopic allergy, New Engl. J. Med., 305, 1551-1559.
776. Marsh W.L. (1978). Chronic granulomatous disease, Kx antigen and the Kell blood groups. In: Brewer G. J. (ed.), Progress in clinical and biological research. The red cell, Vol. 21, Liss, New York, pp. 493-507.
777. Marsh W.L., Oyen R., Nichols M. K, Allen F. H. (1975). Chronic granulomatous dosease and the Kell blood groups, Br. J. Haematol., 29, 247.
778. Massart С., Bussen M., Deschamps I., Hors J., LalouelJ.-M., Dausset J., Cohen D. (1985). A systematic study of HLA class II-ß DNA restriction fragments in insulin-dependent diabetes mellitus, Proc. Natl. Acad. Sei. USA, 82, 3335-3339.
779. Matthiuz P. L., Ihde D., Piazza A., Ceppelini R., Bodmer W.F. (1970). New Approaches to the population genetics and segregation analysis of the HL-A system. In: Terasaki P. (ed.), Histocompatibility Testing, Munksgaard, Kopenhagen, pp. 193-205.
780. Maynard-Smith S., Penrose L. S., Smith С. А. В. (1961). Mathematical tables for research workers in human genetics, J and A Churchill, London.
781. McArthur N. (1953). Statistics in twin birth in Italy, 1949 and 1950, Ann. Eugen, 17, 249.
782. UcClintock B. (1944). The relation of homozygous deficiencies to mutations and allelic series in Maize, Genetics, 29, 478-502.
783. McDevitt H. O. et al. (1972). Genetic control of the immune response, mapping of the Ir-1 locus, J. Exp. Med., 135, 1259-1278.
784. McKusick V.A. (1984). The human gene map 15 november 1983. The morbid anatomy of the human genome, Clin. Genet, 25, 89-123.
785. McMichael A., McDewitt H. (1977). The association between the HLA system and disease, Prog. Med. Genet. (New Series), 2, 39100.
786. Menzel H.-J., Kladetzky R.-G., Assmann G. (1983). Apolipoprotein E polymorphism and coronary artery disease, Arteriosclerosis, 3, 310-315.
787. MétnekiJ., Czeizel A. (1980). Contraceptive
Литература
pills and twins, Acta Genet. Med. Gemellol., 29, 233-236.
788. Migeon B. R., Miller S.C. (1968). Humanmouse somatic cell hybrids with single human chromosome (group E): Link with thymidine kinase activity, Science, 162, 1005-1006.
789. MikiC., Yee S., YasudaN., Morton N.E. (1969). Alltype. In: Morton N. E. (éd.), A genetic program library, The Univ. of Hawaii Press, Honolulu.
790. Milch R.A. (1959). A preliminary note of 47 cases of alcaptonuria occurring in 7 interrelated Dominican families, with an additional comment on two previously reported pedigrees, Acta Genet. (Basel), 9, 123-126.
791. MohrJ. (1954). A study of linkage in man. Opera ex Domo Biologiae Hereditariae Humanae Universitatis 33, Munksgaard, Copenhagen.
792. MohrO.L,, Wridt C. (1919). A new type of hereditary brachyphalangy in man, Carnegie Inst. (Wash.), Publ, Nr. 295, 1-64.
793. Moll P. P. (1982). Alternative genetic models: An application to epilepsy. In: Anderson V. E. et al. (eds.), Genetic basis of the epilepsies, Raven Press, New York, pp. 277-289.
794. Moll P.P., Berry Т.О., Weidman W.H., Ellefson R., Gordson H., Kottke B. A. (1984). Detection of genetic heterogeneity among pedigrees through complex segregation analysis: An application to hypercholesterolemia, Amer J. Hum. Genet., 36, 197-211.
795. March E. T. (1941). Chondrodystrophic dwarfs in Denmark, Opera ex Domo Biologiae Hereditariae Humanae Universitatis Hamiensis 3, Munksgaard, Copenhagen.
796. Morton N.E. (1956). The detection and estimation of linkage between the genes for elliptocytosis and the Rh blood type, Am. J. Hum. Genet., 8, 80-96.
797. Morton N.E. (1957). Further scoring types in sequential tests, with a critical review of autosomal and partial sex linkage in man, Am. J. Hum. Genet., 9, 55-75.
798. Morton N.E. (1955). Sequential tests for the detection of linkage, Am. J. Hum. Genet., 7, 277-318.
799. Morton N.E. (1962). Segregation and linkage. In: Burdette W.J. (ed.), Methodology in human genetics, Holden Day, San Francisco, pp. 17-52.
800. Morton N.E. (1969). Segregation analysis. In: Morton N. E. (ed.), Computer application in genetics, Univ. of Hawaii press, Honolulu, pp. 129-139.
SOI. Morton N.E. (1976). Genetic markers in atherosclerosis: a review, J. Med. Genet., 13, 81-90.
802. Morton N. E. (1983). Outline of genetic epidemiology, S. Karger, Basel etc.
803. Morton N.E., MacLeanC.J. (1974). Analysis of family resemblance III, Complex segregation of quantitative traits, Am. J. Hum. Genet, 26, 489-503.
804. Morton N. E., Yee S., Elston R. C., Lew R.
(1970). Discontinuity and quasi-continuity: Alternative hypothesesof multifactorial inheritance, Clin. Genet., 1, 81-93.
805. Morton N. E., Simpson S. P., Lew R., Yee S. (1983). Estimation of haplotype frequencies. Tissue Antigens, 22, 257-262.
806. Motulsky A.G. (1976). The genetic hyperlipidemias, N. Engl. J. Med., 294, 823-827.
807. Motulsky A.G. (1977). The George M. Kober lecture. A genetical view of modern medicine, Trans Assoc. Am. Physicians., 40, 76-90.
808. Motulsky A.G. (1978). The genetics of common diseases. In: Morton N. E., Chung C. S. (eds.), Genetic epidemiology, Academic Press, New York, pp. 541-548.
809. Motulsky A.G. (1979). The HLA complex and disease. Some interpretations and new data in cardiomyopathy, N. Engl. J. Med., 300, 918919.
810. Motulsky A.G. (1982). Genetic approaches to common diseases. In: Bonné-Tamir B. (ed.), Human Genetics, Part B, Medical Aspects, A Alan R. Liss, New York, pp. 89-95.
811. Motulsky A.G. (1980). Approaches to the genetics of common diseases. In: Rotter J. I., Samloff I. M., Rimoin D. L. (eds.), The Genetics and Heterogeneity of Common Gastrointestinal Disorders, Academic Press, New York, pp. 3-10.
812. Motulsky A.G. (1984). Editorial: Genetic epidemiology, Gen Epidemiol., 1, 143-144.
813. Motulsky A.G. (1984). Genetic research in coronary heart disease. In: Rao D. C., Elston R. C, Kuller L. N., Feinleib M., Carter C., Havlik R. (eds.), Genetic Epidemiology of Coronary Heart Disease, Pasr, Present, and Future, Alan R. Liss, New York, pp. 541-548.
814. Motulsky A.G. (1984). The "new genetics" in blood and cardiovascular research: applications to prevention and treatment, Circulation 70 (Suppl. Ill), III-26-III-30.
815. Motulsky A.G., Boman H. (1975). Genetics and atherosclerosis. In: Schettler G., Weizel A. (eds.), Atherosclerosis, Vol. Ill, Springer, Berlin, pp. 438-444.
816. Motulsky A.G., Boman H. (1975). Screening for the hyperlipidemias. In: Milunsky A. (ed.), The prevention of genetic disease and metal retardation, Saunders, Philadelphia, pp. 306-316.
817. Muhlmann W.E. (1930). Ein ungewöhnlicher Stammbaum über Taubstummheit, Arch. Rassenbiol., 22, 181-183.
818. Munro A., Waldmann H. (1978). The major histocompatibility system and the immune response, Br.Med.Bull., 34, 253-258.
819. Murphy E. A. (1980). The quantitative genetics of disease, Am. J. Med. Genet, 7, 103-113.
820. Murphy E. A. (1981). The genetic dynamics of disease, Am. J. Med. Genet, 8, 35-52.
821. Murphy E. A. (1981). Only authorized persons admitted: The quantitative genetics of health and disease, Johns Hopkins Med. J., 148, 114-122.
822. Murphy E.A. (1982). Muddling, meddling, and modeling. In: Anderson V. E. et al. (eds.),
Литература 271
Genetic basis of the epilepsies, Raven Press, New York, pp. 333-348.
823. Nichtsheim H. (1950). The Feiger anomaly in man and rabbit. A Mendelian character of the nuclei leucocytes, J. Hered., 41, 131-137.
824. NaeslundJ. (1956). Melodiken rid den forsta lasundervisningen. Enoversikt och experimentella bidrag, Svenska, Uppsala.
825. Nance W.E., McConnell P.E. (1973). Status and prospects of research in hereditary deafness, Adv. Hum. Genet, 4, 173-250.
%25a..Nathans J., Piantanida T.P., Eddy Я L., Shows Т. В., HognessD.S. (1986). Molecular genetics of inherited variation in human color vision, Science, 232, 203-210.
826. Neel J. V., Fajons S. S., Com J. W., Davidson R. T. (1965). Diabetes mellitus. In: Neel J. V., Shaw M.W., Schull W.J. (eds.), Genetics and the epidemiology of chronic disease, Govt. Print. Office, Washington, pp. 105-132.
827. Neufeld H.N., Goldbourt U. (1983). Coronary heart disease: genetic aspects, Circulation, 67, 943.
828. Nicholas J.M., Jenkins W.J., Marsh W.L. (1957). Human blood chimeras. A study of surviving twins, Br. Med. J., 1, 1458.
829. NoraJ.J. (1980). Identifying the child at risk coronary heart disease as an adult: a strategy for prevention, J. Pediatr., 97, 706-714.
830. Nora J. J., Lortscher R. H., Spangler R. D., Nora A. H., KimberlingW.J. (1980). Geneticepidemiologic study of early-onset ischémie heart disease, Circulation, 62, 503-508.
831. Olefsky J.M. (1985). Diabetes mellitus. In: Wyngaarden J. В., Smith L. H. Jr. (eds.), Cecil Textbook of Medicine, 17th ed., WB Saunders, Philadelphia, pp. 1320-1341.
831а.Ог/ J. (1974). Estimation of the recombination fraction in human pedifrees: Efficient computation of the likelihood for human linkage studies, Am. J. Hum. Genet., 26, 588-597.
831b.0if J. (1976). A computer program for linkage analysis general human pedigree, Am. J. Hum. Genet, 28, 528-529.
831c.O?iJ. (1977). Counting methods (Em algorithm) in human pedigree analysis. Linkage and segregation analysis, Am. Hum. Genet, 40, 443-454.
832. Fault R.M. (1983). Editorial comment: Dominance and homozygosity in man, Amer J. Med. Genet, 16, 455-458.
833. Pearson K. (1904). On the generalized theory of alternative inheritance with special referenses to Mendel's law, Philos. Trans. R. Soc. A, 203, 53-86.
834. Pearson R.J.C. (1964). Blood groups and disease, Br. Med. J., I, 840.
835. Penrose R.J.C. (1938). (Colchester survey). A clinical and genetic study of 1280 cases of mental defect, HMSO, London, Spec. Rep. Ser. Med. Res. Counc., 229.
836. Penrose L.S. (1947/49). The problem of anticipation in pedigrees of dystrophia myotonica, Ann. Eugen, 14, 125-132.
837. Penrose L.S. (1953). The genetical background
of common disease, Acta Genet. (Basel), 4, 257-265.
838. Petranyi G. G., Irangi P., HollanS.P. (1974). Relations of HL-A and Rh systems to immune reactivity, Vox. Sang., 27, 470-482.
839. Pious D., Erlich H., Gladstone P., Levine F. (1983). Analysis of the HLA region using somatic cell mutants. In: Caskey C.T., White R.L. (eds.), Banbury Report 14, Cold Spring Harbor Laboratory, pp. 61-68.
840. Pola V., Svojitka J. (1957). Klassische Hämophilie bei Frauen, Folia Haematol. (Leipz.), 75, 43-51.
841. PollH. (1914). Über Zwillingsforschung als Hilfsmittel menschlicher Erbkunde, Z. Ethnol., 46, 87-108.
842. Propping P., Kruger J. (1976). Über die Häufigkeit von Zwillingsgeburten, Dtsch. Med. Wochenschr., 101, 506-512.
843. Propping P., Vogel F. (1976). Twin studies in medical genetics, Acta Genet.Med.Gemellol (Roma), 25, 249-258.
844. Propping P., Voigtlander V. (1983). Was ist gesichert in der Genetik der Atopien? Allergologie, 6, 160-168.
845. Puska P., Tuomilehto J., Salonen J. et al. (1979). Changes in coronary risk factors during a comprehensive five-year community programme to control cardiovascular diseases (North Karelia Project), Br. Med. J., 2, 1173-1178.
846. Race R.R., Sanger R. (1969). Xg and sex chromosome abnormalities, Br. Med. Bull., 25, 99-103.
847. Rao C.D., Eiston R.C., Kuller L.H., Femleib M., Carter С., Havlik R. (eds.), (1984). Genetic Epidemiology of Coronary Heart Disease, Past, Present, and Future, Anan. R. Liss, New York.
848. Rappold G., Cremer T., Cremer С., Back W., Bogenberger J., Cooke H.J. (1984). Chromosome assignment of two cloned DNA probes hybridizing predominantly to human sex chromosomes, Hum. Genet, 65, 257-261.
849. Rath B. (1938). Rotgrunblindheit in der Calmbacher Blutersippe. Nachweis des Faktorenaustausches beim Menschen, Arch. Rassenbiol., 32, 397-407.
850. ReedT.E., Neel J. V. (1959). Huntington's chorea in Michigan. 2. Selection and mutation, Am. J. Hum.Genet, 11, 107.
851. Rees A., Shoulders C. C., Stocks J., Galton D.J., Baralle F.E. (1983). DNA polymorphism adjacent to human apoprotein A-I gene: relation to hypertriglyceridemia, Lancet, 1, 444-446.
852. Reich T., Rice J., Cloninger C.R., Wette R., James J. (1979). The use of multiple thresholds and segregation analysis in analyzing the phenotype heterogeniety of multifactorial traits, Ann. Hum. Genet, 42, 371-388.
853. Reid D. H., Parsons P. H. (1963). Sex of parents and variation of recombination with age in the mouse, Heredity, 18, 107.
854. RenwickJ.H. (1956/7). Nail-patella syndrome: Evidence for modification by alleles at the main locus, Ann. Hum. Genet, 21, 159-169.
272 Литература
855. RenwitkJ.H. (1969). Progress m mapping human autosomes, Br. Med. Bull., 25, 65.
856. Richter S. (1967). Zur Heredität des Strabismus concomitans, Humangenetik, 3, 235-243.
857. Richter S. (1966). Untersuchungen über die Heredität des Strabismus concomitans, Sammlung zwangloser Abhandlungen auf dem Gebiet der Augenheilkunde, Thieme, Leipzig.
857а.ЛоШпя D. C., Blix P. M., Rubenstein A. H., Kanazawa Y., Kpsaka K., Tager H.S. (1981). A human proinsulin variant at arginine 65, Nature, 291, 679-681.
858. Robertson F. W. (1981). The genetic component in coronary heart disease - review, Genet. Res. Camb., 37, 1-16.
859. Ro.se N. R., Vladutiu A. O., David C. S., Shreffler D. C. (1973). Autoimmune murine thyroiditis. V. Genetic influence on the disease in BSVS and BRVR mice, Clin. Exp. Immunol., 15, (2), 281-287.
860. Rosenfield R. E., Allen F. H., Rubinstein P. (1973). Genetic model for the Rh blood group system, Proc. Natl. Acad. Sei. USA, 70, 1303-1307.
861. Rotter J. I., Ritnoin D. L. (1981). The genetics of the glucose intolerance disorders, Am. J. Med., 79, 116-126.
862. Rudiger H. W., Drey er M. (1983). Pathogenetic mechanisms of hereditary diabetes mellitus, Hum. Genet., 63, 100-106.
863. Rushton W.A.H. (1975). Visual pigments and color blindness, Sei. Am., 232(3), 64-75.
864. Scott J., KnottT.J., Priestley L. M., Robertson M.E., Mann D. V., Kostner G., Miller G.J., Miller N.E. (1985). High-density lipoprotein composition is altered by a common DNA polymorphism adjacent to apoprotein All gene in man, Lancet, 1, 771-773.
865. Selby P. В., Selby P.R. (1978). Gamma-ray-induced dominant mutations that cause skeletal abnormalities in mice. II. Description of proved mutations, Mutât. Res., 51, 199-236.
866. SheppardP.M. (1975). Natural selection an heredity, 4th ed., Hutchinson, London.
867. Shoelson S., Haneda M., Blix P., Nanjp A., Sänke T., Inouye K., Steiner D., Rubenstein Α., Tager H. (1983). Three mutant insulins in man, Nature, 302, 540-543.
868. Shows T. В., Sakagychi A. Ύ., Naylor S. L. (1982). Mapping the human genome, cloned genes, DNA polymorphism and inherited disease, Adv. Hum. Genet., 12, 341-452.
869. Siemens H. W. (1924). Die Zwillingspathologie, Springer, Berlin.
870. Siemens H. W. (1924). Die Leistungsfähigkeit derzwillingspathologischen Arbeitsmethode, Z. Induktive Abstammungs-Vererbungslehre, 33, 348.
871. Siemens H. W. (1925). Über einen, in der menschlichen Pathologie noch nicht beobachten Vererbungsmodus: Dominant geschlechtsgebundene Vererbung, Arch. RassenbioL, 17, 4761.
872 Simon M., Alexandre J. L., Bourel M., LeMarec B., Scordta C. (1977). Heredity of idiopat-
hic haemochromatosis: a study of 106 families, Clin. Genet., 11, 327-241. 872a.S;mon M., Bourel M., Genetet B., Fauchet R. (1977). Idiopathic hemochromatosis: demonstration of recessive transmission and early detection by family HLA typing, N. Engl. J. Med., 297, 1017-1021.
873. Simonds B. (1963). Tuberculosis in twins, Putnam, London.
874. Sing C.F., Davignon J. (1985). Role of the apolipoprotein E polymorphism in determining normal plasma lipid and lipoprotein variation, Am. J. Hum. Genet., 37,
875. Slack J. (1979). Inheritance of familial hypercholesterolemia. In: Paoletti R., Grott A. M. Jr. (eds.), Atherosclerosis Reviews, Vol. 5, Raven Press, New York, pp. 35-66.
&75a.Smith Ch. (1971). Recurrence risks for multifactorial inheritance. Am. J. Hum. Genet., 23, 578-588.
876. Smith C. A.B. (1956). A test for segregation ratios in family data, Ann. Hum. Genet., 20, 257.
877. Smith C.A.B. (1956/7). Counting methods in genetical statistics, Ann. Hum. Genet., 21, 254-276.
878. Smith C.A.B. (1959). A note on the effect of ascertainment on segregation ratios, Ann. Hum. Genet, 23, 311-323.
879. Smith C. A. B. (1970). A note on testing the Hardy-Weinberg law, Ann. Hum. Genet., 33, 377.
880. Smith C.H. (1970). Heritability of liability and concordance in monozygous twins, Ann. Hum. Genet., 34, 85.
881. Smith S.M., Penrose L.S. (1955). Monozygotic and dizygotic twin diagnosis, Ann. Hum. Genet., 19, 273-289.
882. Smith S.M., Penrose L.S., Smith C.A.B. (1961). Mathematical tables for research workers in human genetics, Churchill, London.
883. Smithies O. (1964). Chromosomal rearrangements and protein structure, Cold Spring Harbor Symp. Quant. Biol, 29, 309.
884. Smithies O., Cornell G. E., DixonG.H. (1962). Chromosomal rearrangements and the evolution of haptoglobin genes, Nature, 196, 232.
885. Snyder L.F., Doan C.A. (1944). Is the homozygous form of multiple teleangiectasia lethal? Lab. Clin. Med., 29. 1211-1216.
886. Sorensen H., Dissing J. (1975a). Association between the C3F gene and atherosclerotic vascular diseases, Hum. Hered., 25, 279-283.
887. Southern E. M. (1982). Application of DNA analysis to mapping the human genome, Cytogenet. Cell Genet., 32, 52-57.
888. Svejgaard A., Jersild C., Staub Nielsen L., Bodmer W.F. (1974). HL-A antigens and disease. Statistical and genetical considerations, Tissue Antigens, 4, 95-105.
889. Svejgaard A., Hauge M., Jersild C., Platz P., Ryder L. P., Staub Nielsen L., Thomsen M. (1979). The HLA system. An introductory survey, 2nd ed., Karger, Basel, New York.
890. Swanson J., Park В., McCullough J. (1972).
Литература 273
Kell phenotypes in families of patients with X-linked chronic granulomatous disease, 12th Congress of the International Society for Blood Transfusion, Washington (Abstracts), p. 26.
Ш. Schaefer E.J. (1984). Clinical, biochemical, and genetic features in familial disorders of high density lipoprotein deficiency, Arteriosclerosis, 4, 303-322.
Ä92. Schepank H. (1974). Erb- und Umweltfactoren bei Neurosen, Psychiatry Series, 11, 1-221.
Ш. Schiff F., v Versöhner 0. (1933). Serologische Untersuchungen an Zwillingen. II. Mitt.Z.MorphoLAnthropol, 32, 244-249.
894. Schnyder U. W. (1955). Neirodermitis und Allergie des Respirationstraktes, Dermatologica, 110, 289.
895. Schroeder T.-M., Tilgen D., Kruger J., Vogel F. (1976). Formal genetics of Fanconi's anemia, Hum.Genet., 32, 257-288.
№a.Schrott H. G., Karp L., OmennG.S. (1973). Prenatal prediction in myotonic dystrophy: guidelines for genetic counseling, Clin. Genet., 4, 38-45.
896. Steinberg A.G. (1965). Evidence for a mutation or crossing over at the Rh-locus, Vox Sang, 10, 721.
897. Stern C. (1957). The problem of complete Y-lihkage in man, Am. J. Hum.Genet, 9, 147-165.
898. Stern C., Walls G.L. (1957). The Cunier pedigree of "color blindness", Am. J. Hum. Genet, 9, 249-273.
899. Stevenson A.C., Cheeseman E.A. (1955/56). Hereditary deaf mutism with particular reference to Northern Ireland, Ann. Hum. Genet., 20, 177-231.
900. Stevens W.L. (1950). Statistical analysis of the ABO blood groups, Hum. Biol., 22, 191217.
901. Stocks P., Barrington A. (1925). Hereditary disorders of bone development, Treasury of Human Inheritance 3, Part I.
902. Stone N.J. (1979). Genetic hyperdipidemia and atherosclerosis, Artery, 5, 377-397.
903. Strasser G. (1982). Coronary risk factors revisited, World Health Forum, 3, 85-88.
904. Sturtevant A. H. (1925). The effect of unequal crossing over at the bar locus in drosophila, Genetics, 10, 117.
№a.Svejgaard A., Platz P., Ryder L. P. (1983). HLA and disease 1982. In: Möller G. (ed.), HLA and disease susceptibility (Immunological reviews, vol. 70), Munksgaard, Copenhagen, pp. 193-218.
905. Tattersall R. (1976). The inheritance of maturity-onset type diabetes in young people. In: Creutzfeldt E., Kobberling J., Neel J. V. (eds.), The genetics of diabetes mellitus, Springer Verlag, Berlin, Heidelberg, New York, pp. 88-95.
906. Tattersall R. B., PykeD.A. (1972). Diabetes in identical twins, Lancet, II, 1120-1125.
907. ten Kate L. P., Boman H., Daiger S. P., Motulsky A.G. (1982). Familial aggregation of coronary heart disease and its relation to known
genetic risk factors, Am. J. Cardiol., 50, 945953.
908. ten Kate L. P., Boman H., Daiger S. P., Motulsky A.G, (1984). Increased frequency of coronary heart disease in relatives of wives of myocardial infarct survivors: assortative mating for lifestyle and risk factors, Am. J. Cardiol., 53, 399-403.
910. Terasaki P.I. (1980). Histocompatibility testing 1980, UCLA Tissue Typing Laboratory, Los Angeles.
911. Terasaki P. I., McClelland J. D. (1964). Microdroplet assay of human serum cytotoxins, Nature, 204, 998-1000.
912. Timoftef-Ressovsky N. W. (1931). Gerichtetes Variieren in der Phänotypischen Manifestierung einiger Generationen von Drosophila funebris, Naturwissenschaften, 19, 493-497.
913. Tolleshaung. H., Goldstein J.L., Schneider W.J., Brown M. S. (1982). Posttranslational processing of the LDL receptor and ist genetic disruption in familial hypercholesterolemia, Cell, 30, 715-724.
914. Trevor-Roper P.D. (1952). Marriage of two complete albinos with normally pigmented offspring, Br. J. Ophthalmol., 36, 107.
915. Utermann G. (1983). Coronary heart disease. In: Emery A.E.H., Rimoin D. L. (eds.), Principles and practice of medical genetics, Churchill Livingstone, Edinburgh etc., pp. 956-978.
916. Utermann G., Hardewig Α., Zimmer F. (1984). Apolipoprotein E phenotypes in patients with myocardial infarction, Hum. Genet, 65, 237241.
917. Utermann G., Kindermann L, Kaffarnik H., Steinmetz A. (1984). Apolipoprotein E phenotypes and hyperlipidemia, Hum. Genêt, 65, 232-236.
918. Verschuer O. von (1954). Wirksame Faktoren im Leben des Menschen, Steiner, Wiesbaden.
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