АкушерствоАнатомияАнестезиологияВакцинопрофилактикаВалеологияВетеринарияГигиенаЗаболеванияИммунологияКардиологияНеврологияНефрологияОнкологияОториноларингологияОфтальмологияПаразитологияПедиатрияПервая помощьПсихиатрияПульмонологияРеанимацияРевматологияСтоматологияТерапияТоксикологияТравматологияУрологияФармакологияФармацевтикаФизиотерапияФтизиатрияХирургияЭндокринологияЭпидемиология

Приложение 8. 239 5 страница

579. Birch-Jensen A. (1949). Congenital deformities of the upper extremities, Opera ex Domo Biologiae Hereditariae Humanae Universitatis

Hafniensis Munksgaard, Kopenhagen, 19.

580. Blackburn H. (1979). Diet and mass hyperlipidemia: a public health view. In: Levy R., Rifkind В., Dennis В., Ernst N. (eds.), Nutrition, Lipids, and Coronary Heart Disease, Raven Press, New York.

581. Bodmer W.F. (1972). Population genetics of the HL-A System: Retrospect and prospect. In: Dausset J., Colombani J. (eds.), Histocompatibility testing, Munksgaard, Copenhagen, pp. 611—617.

582. Bodmer W.F,, Bodmer J.G. (1978). Evolution and function of the HLA system, Br. Med. Bull, 34, 390-316.

583. Boman H., Ott J., Hazzard W.R., Albers J.J., Cooper M.N., Motulsky A.G. (1978). Familial hyperlipidemia in 95 randomly ascertained hyperlipidemic men, Clin. Genet, 13, 108.

584. Botstein D., White R.L., Skolnick M., Davis R. W. (1980). Construction of a genetic linkage map in man using restriction fragment length polymorphism, Am. J. Hum. Genet, 32, 314-331.

5&4a. Bowman B.H., Kurosky A. (1982). Haptoglobin: The evolutionary product of duplication, unequal crossing over, and point mutation. In: Harris H., Hirschhorn K. (eds.), Advances in Human Genetics, Vol. 12, Plenum Press, New York and London, pp. 189-261.

585. Boyd W. C. (1955). Maximum likelihood estimation of Rh gene frequencies in Pacific populations, Nature, 176, 648.

586. Boyd W.C. (1955). Simple maximum likelihood method for calculating Rh gene frequencies in Pacific populations, Am. J. Phys. Anthrop., 13, 447-453.

587. Bracken H. von (1934). Mutual intimacy in twins: Types of structure in pairs of identical and fraternal twins, Character and Personality, 2, 293-309.

588. Bridges C.B. (1936). The bar "gene", a duplication, Science, 83, 210.

589. Bridges R. A., Berendes H., Good R. A. (1959). A fatal granulomatous disease of childhood, Am. J. Dis. Child., 97, 387.

590. Bronnes tarn R. (1973a). Studies on the C3 polymorphism. Relation between phenotype and quantitative immunochemical measurements, Hum. Hered., 23, 128-134.

591. Bronnestam R. (1973b). Studies on the C3 polymorphism. Relationship between C3 phenotype and rheumatoid arthritis, Hum. Hered., 23, 206-213.

592. Brown M.S., Goldstein J.L., (1979). Abetalipoproteinemia. In: Goodman R. M., Motulsky A. G. (eds.), Genetic diseases among Ashkenazi Jews, Raven, New York.

593. Brown M.S., Goldstein J.L. (1984). How LDL receptors influence cholesterol and atherosclerosis, Sei. Am., 251, 58-66.

594. BrunzellJ.D., Schrott H. G., Motulsky A. G., Bierman E. L. (1976). Myocardial infarction in the familial forms of hypertriglyceridemia, Metabolism, 25, 313-320.

595. Burke W. Hornung S., Copeland B. R., Fur-

264 Литература

long С. E., Motulsky A. G. (1984). Red cell sodium-lithium countertransport in hypertension. In: Villarreal H., Sambhi M. P. (eds.), Topics in Pathophysiology of Hypertension, Martinus Nijhoff Boston, pp. 88 99.

596. Burke W., Motulsky A. G. (1985). Genetics of hypertension, Pract. Cardiol., 11, 159-173.

597. Burke W., Motulsky A. G. (1985). Hypertension-some unanswered questions, JAMA, 253, 2260-2261.

598. Cagianit В., Rhyner K., Furrer W., Schnebli H.P. (1981). Thiosulfate- sulphur transferase (Rhodanase) deficiency in Leber's hereditary optic atrophy, Lancet, II, 981-982.

599. Carney R.G.,jr. (1976). Incontinentia pigmenti: A world statistical analysis, Arch. Dermatol., 112, 535-542.

600. Carter C.O. (1969). Genetics of common disorders, Brit. Med. Bull., 25, 52-57.

601. Carter C.O. (1961). The inheritance of congenital pyloric stenosis, Br. Med. Bull., 17, 251-254.

602. Canter C.O. (1976). Genetics of common single malformation, Br. Med. Bull., 32, 21-26.

603. Carter C.O. (1977). Genetic of common diseases. In: Gene-environment interaction in cohimon diseases, Japan Medical Research Foundation (éd.), pp. 108-117, University of Tokyo Press, Tokyo.

604. Caskey С. Т. (1985). New aid to human gene mapping, Nature, 314, 19.

605. Ceppellini R., Dunn L. C., Turri M. (1955). An interaction between alleles at the Rh locus in man which weakens the reactivity of the Rh₀ factor (D"), Proc. Natl. Acad. Sei. USA, 41, 283-288.

606. Ceppellini R. L., Siniscalco M. (1955). Una nuova ipotesi genetica per il sistema Lewissecretore e suoi refiessi nei reguardi di alcune evidenze di linkage con altri loci, Riv. 1st. sieroter Ital, 30, 431-445.

607. Ceppellini R., Siniscalo M., Smith С. А. В. (1955/56). The estimation of gene frequencies in a random-mating population, Ann. Hum. Genet., 20, 97.

608. Chakravartti M. R., Vogel F. (1973). Topics in human genetics, Vol. I, A twin study on leprosy, Thieme, Stuttgart.

609. Chown В., Lewis M., Hiroko K. (1957). A "new" Kell blood group phenotype, Nature, 180, 711.

610. Chung C.S., Morton N.E. (1959). Discrimination of genetic entities in muscular dystrophy, Am. J. Hum. Genet., 11, 339-359.

611. Cloninger C.R., Rice J., Reich Th., McGriffin P. (1982). Genetic analysis of seizure disorders as multidimensional threshold characters. In: Anderson V. E. (ed.), Genetic basis of the epilepsies, Raven Press, New York, pp. 291-309.

612. Cohen-Hagenauer O., Robbins E., Messart С., Busson M., Deschamps I., Hors J., Lalouel J.-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.

612a. Coneally P. M., Rivas M. L. (1980). Linkage analysis in man, Adv. in Hum. Genet., 10, 209-266.

612b. Cook P.J.L., RobsonE.B., BucktonK.E., Jacobs P. A., PolaniP.E. (1974). Segregation of genetic markers infamilies with chromosome polymorphisms and structural rearrangements involving chromosome 1, Ann. Hum. Genet., 37, 261-274.

613. Carney G., Seedburgh D., Thompson В., Campbell D.M., Mac GillivrayL, Timlin D. (1979). Maternal Height and Twinning, Ann. Hum. Genet., 43, 55-59.

614. Cudworth A.G., Wolf E. (1982). The genetic susceptibility to type I (insulin-dependent) diabetes mellitus, Clin. Endocr. Metab., 11, 389-408 1.

615. Cuënot L. (1905). Les races pures et leur combinaisons chez les souris, Arch. Zool. Exp. Genêt., 3, 123-132.

616. Czeizel A. (1978). The Hungarian congenital malformation monitoring system, Acta Раеdiät. Academ. Seientiarum Hungaricae, 19, 225—238

617. Czeizel A., Kiss P., Oszotovics M. et al. (1978). Nationwide investigations of multiple malformations, Acta Paediat Academ. Scientiarum Hungaricae, 19, 275-280.

618. Czeizel A., Pazonyi 1., Métreki J., Tomka M. (1979). The first five years of the budapest twin register, 1970-1974, Acta Genet. Med. Gemellol, 28, 73-76.

619. Czeizel A., Tusnady G., Vaczo G., Vizkelety T. (1975). The mechanism of genetic predisposition in congenital dislocation of the hip, J. Med. Genet, 12, 121-124.

620. DalgaardO.Z. (1957). Bilateral polycystic disease of the kidneys, Opera ex Domo, Biologiae Hereditariae Humanae Universitatis hafniensis Munksgaard, Copenhagen, 38, 255 pp.

621. Das N.K., Biro P.A., Duceman В., Sood A.K., Shyma E., Ready P., Lawrance S., Pan J., WeissmanS.M. (1983). Molecular studies of the genes of the human major histocompatibility. In; Caskey C.T., White R.L. (eds.), Banbury Report 14, Cold Spring Harbor Lab., p. 41-51.

622. Dausset J., Colombani J. (1972). Histocompatibility testing 1972, Munksgaard, Copenhagen.

623. Dausset J., Contu L. (1980). The MHC and immune response in man, Progr. Immunol., 4, 513-529.

624. Davies K. E., Young B. D., Elles R. G., Hill U.E., Williamson R. (1981). Cloning of a representative genomic library of the human X chromosome after sorting by flow cytometry, Nature, 293,' 374-376.

625. Davis S.H., Gavin J., Goldsmith K.L.G., Graham J. В., Hamper J., Hardisty R. M., Harris J. В., Holman C. A., Ingram G. I. C., Jones T.G., McAfee L.A., McKusick V.A., O'Brien J. R., Race R. R., Sanger R., Tippett P.

Литература 265

(1963). The linkage relations of hemophilia A and hemophilia B (christmas disease) to the Xg blood group system, Am. J. Hum. Genet, 15, 481 492.

626. Deeb S.S., Motulsky A.G., Albers J.J. (1985). A partial cDNA clone for human apolipoprotein B, Proc. Natl. Acad. Sei. USA, 82, 4983-4986.

627. Degnbol В., Green A. (1978). Diabetes mellitus among first- and second-degree relatives of early onset diabetics, Ann. Hum. Genet, 42, 25-47.

628. Demenais F., Bonaiti С., Briard M.-L., Feingold J., Frezal J. (1979). Congenital glaucoma: Genetic models, Hum. Genet, 46, 305-317.

629. Domahue R. P., Bias W.B., RenwickJ.H., McKusick V.A. (1968). Probable assignment of the Duffy bloodgroup locus to chromosome 1 in man. Proc. Natl. Acad. Sei. USA, 61, 949.

630. Dorn H. (1959). Xeroderma pigmentosum, Acta Genet Med. Gemellol (Roma), 8, 395-408.

631. Dungern E. von, Hirzfeld L. (1911). Über gruppenspezifische Structuren des Blutes. III. Z. Immunitatsforsch., 8, 526-562.

632. Dunsford L, Bowley C. C., Hutchinson A. M., Thompson J. S., Sanger R., Race R. R. (1953). A human bloodgroup chimera, Br. Med. J., II, 81.

633. Dupont В., Smithwick E. M., Oberfleld S. E., Lee T-D., Levine L.S. (1977). Close genetic linkage between HLA and congenital adrenal hyperplasia (21-hydroxylase deficiency), Lancet, II, 1309-1312.

634. Eaves L.J. (1982). The utility of twins. In: Anderson V. E. et al. (eds.), Genetic basis of the epilepsies, Raven Press, New York, pp. 249-276.

635. Eder H.A., Gidez L.J. (1982). The clinical significance of the plasma high density lipoproteins, Med. Clin. North Am., 66, 431440.

636. Edwards J.H. (1960). The simulation of mendelism, Acta Genet., (Basel), 10, 63-70.

637. Edwards J.H. (1965). The meaning of the associations between blood group and disease, Am. J. Hum. Genet, 29, 77.

638. Edwards J. A., Gale R. P. (1972). Camptobrachydactyly: A new autosomal sominant trait with two probable homozygotes, Amer. J. Hum. Genet, 24, 464 474.

639. Egger J., Wilson J. (1983). Mitochondrial inheritance in a mitochondrially mediated disease, New England Journal Med., 309, 142-146.

640. Ehling U.H. (1966). Dominant mutations of the skeleton in off spring of X-irratiated male mice, Genetics, 54, 1381-1389.

641. Ehling U.H. (1970). Evaluation of presumed dominant skeletal mutation. In: Vogel F., Röhrborn G. (eds.), Chemical mutagenesis in mammals and man, Springer, Berlin, Heidelberg, New York, pp. 162-166.

642. Ehling U.H., Randolph M. L. (1962). Skeletal abnormalities in the F, generation of mice

exposed to ionizing radiations, Genetics, 47, 1543-1555.

643. Eichwald E.J., Silmser C.R. (1955). Communication, Transplant. Bull., 2, 148 149.

644. Ellison R. T. Ill, Kohler P. F., Curd J. G., JudsonF.N., Relier L.B. (1983). Prevalence of congenital or acquired complement deficiency in patients with sporadic meningococcal disease, N. Engl. J. Med., 308, 913-916.

645. Elsas L.J., Endo F., S trumlauf E., Elders J., Priest J. H. (1985). Leprechaunism: a inherited defect in a highaffinity insulin receptor, Am. Hum. Genet., 37, 73-88.

646. Eiston R. С. (1979). Major locus analysis for quantitative trains, Amer. J. Hum. Genet, 31, 655-661.

647. Eiston R.C. (1981). Segregation analysis, Adv. in Hum. Genet, 11, 63 120.

648. Elston R. C., Classman E. (1967). An aproach to the problem of whether clustering of functionally related genes occurs in higher organisms, Genet Res. (London), 9, 141-147.

649. Elston J.H., Lange K. (1975). The prior probability of autosomal linkage, Ann. Hum. Genet, 38, 341-350.

650. Epstein F.H. (1976). Genetics of ischémie heart disease, Postgrad. Med., J., 52, 477-480.

651. Eriksson S. (1965). Studies in alpha 1-antitrypsin deficiency, Acta Med. Scand., 177, 175.

652. Erlich H., Stetler D., Grumet C. (1983). Restriction length polymorphism analysis of HLA-typed families using cloned HLA probes. In: Caskey C.T., White R.L. (Eds.), Banbury Report 14, Cold Spring Harbor Lab., pp. 327-334.

653. Fagerhol M.K., Cox D. W. (1981). The Pi polymorphism: Genetics, biochemical and clinical aspects of human alpha j-antitrypsin, Adv. in Hum. Genet, 11, 1-62.

654. Falconer D.S. (1965). The inheritance of liability to certain diseases, estimated from the incidence among relatives, Ann. Hum. Genet, 29, 51.

655. Falconer D.S. (1967). The inheritance of liability to diseases with variable age of onset with particular reference to diabetes mellitus, Ann. Hum. Genet, 31, 1-20.

656. Farabee (1905). Inheritance of digital malformations in man, Papers of the Peabody Museum for Americal Archeology and Ethnology (Harvard University), 3, 69.

657. Farhud D. В., Ananthakrishnan R., Walter H. (1972). Association between the C3 phenotypes and various diseases, Hum. Genet, 17, 57-60.

658. Farquhar J. W., Maccoby N.. Wood P. D., Alexander J. K., Breitrose H., Brown B. W. ir., HaskellW.L., Me Allster A. L., Meyer A. J., NashJ.D., Stern M. P. (1977). Community education for cardiovascular health, Lancet, 1, 1192-1195.

659. Felle W. (1950). An introduction to probability theory and its applications, John Wiley and Sons, New York.

660. Ferns G. A. A., Stocks J., Ritchie C., Gal-

Литература

ton D. J. (1985). Genetic polymorphisms of apolipoprotein C-III and insulin in survivors of myocardial infarction, Lancet, 2, 300303.

661. Fialkow P.J., Giblett E.R., Motulsky A.G. (1967). Measurable linkage between ocular albinism and Xg, Am. J. Hum. Genet, 19, 63-69.

662. FinkelsteinS., Walford R.L., Myers L. W., Ellison G. W. (1974). HL-A antigens and hypersensitivity to brain tissue in multiple sclerosis, Lancet, I, 736.

663. Finney D.J. (1947/9). The truncated binomial distribution, Ann. Eugen., 14, 319-328.

664. Fischer R.A. (1918). The correlation between relatives on the supposition of Mendelian inheritance, Trans. R. Soc. (Edinburgh), 52, 399-433.

665. Fischer R.A., Race R.R. (1946). Rh gene frequencies in Britain, Nature, 157, 8.

666. Flodents Y., Iselius L., Lindsten J., Wetterburg L. (1982). Evidence for a major locus as well as a multifactorial component in the regulation of human red blood cell catechol0-methyltransferase activity, Hum Hered., 32, 76-79.

667. Folstein S. K, Phillips J. A. Ill, Meyers D. A., Chase G. A., Abbott M.H., Franz M.L., Waber P. G., Kazazian H. H. Jr., Conneally P. M., Hobbs W., Tanzi R., Faryniarz A., Gibbons K., Gussella J. (1985). Huntingdon's disease: two families with differing clinical features show linkage to the G8 probe, Science, 229, 776-779.

668. Franceschetti A., Klein D. (1957). Two families with parents of different types of red-green blindness, Acta Genet. (Basel), 7, 255.

669. Fraser G.R. (1976). The cause of profound deafness in childhood, Johns Hopkins University Press, Baltimore, London.

670. Fraser G.R., Friedman A.I. (1967). The causes of blindness in с chindhood, Johns Hopkins University Press, Baltimore.

671. Fredrickson D.S., Goldstein J.L., Brown M.S. (1978). The familian hyperlipoproteinemias. In: Stanbury J. В., Wyngaarden J. В., Fredrickson D. S. (eds.), The Metabolic Basis of Inherited Disease, 4th ed., McGraw-Hill, New York, pp. 604-655.

672. Fuhrmann W. (1963). Das Syndrom der erblichen Nephropathie mit Innenohrschwerhorigkeit (Alport-Syndrom), Dtsch. Med, Wochenschr., 88, 525-532.

673. Fuhrmann W. (1974). Die formale Genetik des Menschen. In: Vogel F. (ed.), Handbuch der Allgemeinen Pathologie, Vol. IX, Erbgefüge, Springer, Berlin, Heidelberg, New York, pp. 147-259.

674. Fuhrmann W, Stahl A., Schroeder T. M. (1966). Das oro-facio-digitale Syndrom, Humangenetik, 2, 133-164.

675. Galton F. (1876). The history of twins as a critérium of the relative powers of nature, J. Anthropol. Inst.

676. Gartler S. M., Francke U. (1975). Half chroma-

tid mutations: Transmission in humans? Am. J. Hum. Genet, 27, 218-223.

677. GaulL.E. (1953). Heredity of multiple benign cystic epithelioma, Arch. Dermatol. Syph. (Chicago), 68, 517.

678. Gelb A. F., Klein E., Lieberman J. (1977). Pulmonary function in nonsmoking subjects with alpha! antitrypsin deficiency (MZ phenotype), Am. J. Med., 62, 93.

679. Gerard G., Vitrac D., Le Pendu J., Muller Α., Oriol R. (1982). Η-deficient blood groups (Bombay) of Reunion island, Amer. J. Hum. Genet, 34, 937-947.

680. Gesell Α., Thompson H. (1929). Learning and growth in identical infant twins: An experimental study by the method of co-twin control, Genet. Psychol. Monogr., 6, 5-124.

681. Gey er E. (1940). Ein Zwillingspärchen mit zwei Vätern. Arch. Rassenbiol., 34, 226-236.

682. Giblett E. R., Klebanoff S. J., Pincus S. H., Swanson J., Park B. H., McCullough J. (1971). Kell phenotypes in chronic granulomatous disease: a potential transfusion hazard, Lancet, I, 1235.

683. Goldberg A.S. (1978). Pitfalls in the resolution of I. Q. inheritance, pp. 195-222, In: Morton N. E., Chung C. S. (eds.), Genetic epidemiology, Academic Press, New York etc.

684. Goldstein J.L., Brown M.S. (1977). Atherosclerosis: thelow-density lipoprotein receptor hypothesis, Metabolism, 26, 1257-1275.

685. Goldstein J.L., Brown M.S. (1979). LDL receptor defectin familial hypercholesterolemia, Med. Clin. North Am., 66, 335-362.

686. Goldstein J.L., HazzardW.R., Schrott H. G., Bierman E. L., Motulsky A. G. (1973). Hyperlipidemia in coronary heart disease. II. Genetic analysis of lipid levels in 176 families and delineation of a new inherited disorder, J. Clin Invest, 54, 1544-1568.

687. Grebe H. (1959). Erblicher Zwergwuchs, Ergeb. Inn. Med. Kinderheilkd., 12, 343-427.

688. Greiner J., Schleiermacher E., Smith T., Lenhard V., Vogel F. (1978). The HLA system and leprosy in Thailand, Hum. Genet., 42, 201-213.

688a. Greiner J., Kruger J., Palden L., Jung E. G., Vogel F. (1983). A linkage study of acrokeratoelastoidosis, Possible mapping to chromosome 2, Hum. Genet, 63, 222-227.

689. Grosse-Wilde H., Bertrams J., Schuppten W., Netzel B., Kuppelt W., Kuwert E.K. (1977). HLA-D typing in 111 multiple sclerosis patients: Distribution of four HLA-D alleles, Immunogenetics, 4, 481-488.

690. Gruneberg H. (1952). Quasi-continuous variations in the mouse, Symp. Genet, 3, 215-227.

691. Gruneberg H. (1952). Genetical studies in the skeleton of the mouse. IV. Quasi-continuous variations, J. Genet, 51, 95-114.

692. Girzeschik K.-H. (1973). Utilization of mosaic cellhypbrids for genetic studies in man, Hum. Genet, 19, 1-40.

693. Gusella J. F., Tanzi R. E., Anderson Μ. Α., Hobbs W., Gibbons K., Raschtchian R., Gilli-

Литература 267

am Т.С., Wallace M. R., Wexler N. S., Conneally P. M. (1984). DNA markers for nervous system diseases, Science, 225, 1320-1326.

694. Gusella J. F., Wexler N. S., Conneally P.M., Naylor S. L., Anderson M. Α., Tanzi R. E., Watkins P. С., Ottina С., Wallace M. R., Sakaguchi A. Y., Young А. В., Shoulson I., BonillaE., Martin J.B. (1983). A polymorphic DNA marker genetically linked to Huntington's disease, Nature, 306, 234-238.

695. HaaseF.H. (1938/39). Die Übersterblichkeit der Knaben als Folge recessiver geschlechtsgebundener Anlagen, Z. Menschl. Vererbungs-Konstitutionslehre, 22, 105-126.

696. Hadorn E. (1955). Developmental genetics and lethal factors, John Wiley and Sons, London, New York.

697. Haldane J.B.S. (1941). The relative importance of principal and modifying genes in determining some human diseases, J. Genet, 41, 149-157.

698. Haldane J.B.S., Smith C. A.B. (1947/9). A simple exact test for birth order effect, Ann. Eugen., 14, 116-122.

699. Haldane J.B.S., Smith C.A.B. (1947). A new estimate of the linkagebetween the genes for color blindness and haemophilia in man, Ann. Eugen., 14, 10-31.

700. Hall J. G., Dorst J. P., Taybi H., Scott C. I., Langer L. О., McKusick V. A. (1969). Two probable cases of homozygosity for the achondroplasia gene, Birth Defects, 4, 24-34.

701. Hornby R.I. (1981). Hereditary aspects of coronary artery disease, Am. Heart. J., 101, 639-649.

702. Harris H. (1970). Cell fusion, Clarendon, Oxford.

702a. Harris H. (1948). A sex-limiting modifying gene in diaphyseal aclasis (multiple exostoses), Ann. Eugen, 14, 165-170.

703. Harris H., Smith C.A.B. (1948). The sib-sib age of onset correlation among individuals suffering from a hereditary syndrome produced by more than one gene, Ann. Eugen, 14, 309-318.

704. HatzoldO. (1966). Die Sexualproportion der Geborenen und ihre Schwankungen als präkonzeptionelles Wahrscheinlichkeitsproblem, Dtsch. Akad. f Bevölkerungswissenschaft, Reihe B., Vol. 5.

705. Hauge M., Harvald B., Fischer M., GottliebJensen K., Juel: nielsen N., Raebild I., Shapiro R., Videbech T. (1968). The Danish twin register, Aota Genet. Med. Gemellol (Roma), 18, 315-332.

706. Havel R. J. (1982). Familial dysbetalipoproteinemia, Med. Clin. North Am., 66, 441-454.

707. Haverkamp-Begemann N., Lookeren-Campagne van A (1952). Homozygous from of Feiger Huet's nuclear anomaly in man, Acta Haematol (Basel), 7, 295-303.

708. Haws D. V., McKusick V. A. (1963). Farabee's brachydactylous kindred revisited, Johns Hopkins Med. J., 113, 20-30.

709. Hegemon J.P., Mash A.J., Spivey B.E. (1974). Genetic analysis of human visual parameters in populations with varying incidence of strabism, Am. J. Hum. Genet., 26, 549-562.

710. Helmbold W. (1959). Über den möglichen Aufbau des Rh-Genkomplexes, Blut, 5, 141-148.

711. Helmbold W., Prokop 0. (1958). Die Bestimmung der ABO-Genfrequenzen mittels der maximum-likelihood-Methode und anderer Verfahren anhand forensischer Blutgruppenbestimmungen in Berlin, Blut, 4, 190-201.

712. Hershon K., Brunzell J., Albers J.J., Haas L., Motulsky A. (1981). Hyper-apo-B-lipoproteinemia with variable lipid phenotype (familial combined hyperlipidernia). Arterosclerosis, l, 380a.

712a. Hirszfeld L. (1928). Konstitutionsserologie und Blutgruppenforschung, Springer, Berlin.

713. Hitman G. Α., Jowett N. I., Williams L. G., Humphries S., Winter R. M., Galton D. J. (1984). Polymorphism in the 5'-flamking region of the insulin gene and non-insulindependent diabetes, Clin. Sei., 66, 383-388.

714. Hitzig W. H., Seger R. A. (1983). Chronic granulanatous disease, a heterogenous syndrome, Hum. Genet., 64, 207-215.

715. Holmes В., Quie P.G., Windhorst D. В., Good R. А. (1966). Fatal granulomatous disease of childhood: an inborn abnormality of phagocytic function, Lancet, I, 1225.

716. Howell-Evans W., McConnel R.B., Clarke C.A., SheppardP.M. (1958). Carcinoma of the oesophagus with keratosis palmaris and plantaris (tylosis), Q.J. Med. (new series), 27, 413-429.

717. HrubecZ., Robinette C.D. (1984). The study of human twins in medical research, N. Engl. J., Med., 310, 435-441.

718. Hully S.B., Rosenman R.H., Bawol R.D., Brand R. J. (1980). Epidemiology as a guide to clinical decisions. The association between triglycéride and coronary heart disease, N. Engl. J. Med., 302, 1383-1389.

719. Humphries S.E., Kessling A.M., Horsthemke В., Donald J. Α., Seed M., Jowett N.. Holm M., Galton D.J., Wynn V., Williamson R. (1985). A common DNA polymorphism of the low-density lipoprotein (LDL) receptor gene and its use in diagnosis, Lancet, 1, 10031005.

720. Hülfen M. (1974). Chiasma distribution at diakinesis in the normal human male, Hereditas, 76, 55-78.

721. Husén T. (1959). Psychological twin research, Almquist and Wiksell, Stockholm.

722. Illingworth D. R., Sexton G. J. (1984). Hypocholesterolemic effects of mevinolin in patients with heterozygous familial hyperholesterolemia, J. Clin. Invest., 74, 1972-1978.

723. Inkeles S., Eisenberg D. (1981). Hyperlipidernia and coronary atherosclerosis: a review, Medicine, 60, 110-123.

724. IseliusL., LalouelJ.M. (1982). Complex segregation analysis of hyperalphalipoproteinemia, Metabolism, 31, 521-523.

268 Литература

725. Jackson J. l·'., Currier R. D., Terasaki P. L, M or ton N. E. (1977). Spinocerebellar ataxia and HLA linkage. Risk prediction by HLA typing, N. Engl. J. Med., 296, 1138-1141.

726. Johannsen W. (1909). Elemente der exakten Erblichkeitslehre, G. Fischer (3rd ed., 1926), Jena.

727. Johnson B. C., Epstein F. H., Kjelsberg M. O. (1965). Distribution and familial studies of blood pressure and serum cholesterol levels in a total community - Tecumseh, Michigan, J. Chron. Dis., 18, 147.

728. Jörgensen G. (1974). Erbfaktoren bie häufigen Krankheiten. In: Vogel F. (ed.), Handbuch der allgemeinen Pathologie, Vol. IX, Erbgefuge, Springer, Berlin, Heidelberg, New York, pp. 581 665.

729. Kaelin A. (1955). Statistische Prüf-und Schätzverfahren für die relative haufigkeit von Merkmalsträgern bei einem der Auslese unterworfenen Merkmal mit Anwendung auf das Retinagliom, Arch. Julius Klaus Stiftung Vererbungsforsch., 30, 263-485.

729a. Kampe O., Larhammer D., Wiwan K., Scheming L., Claesson L.,Gustafsson K., Paabo S., Hyldig - Nielsen J. J., Rask L., Peterson P. A. (1983). Molecular analysis of MHC antigens. In: Möller E., Möller G. (eds.), Genetics of the immune response, Plenum, 001 York, pp. 61 -79.

730. Кадет Α., Rhoads G. С., Zeegan P. D., Nichaman M. Z. (1971). Coronary heart disease among men of Japanese ancestry in Hawaii: the Honolulu heart study, Isr. J. Med., Sei., 7, 1573.

731. KallmannF.J. (1938). The genetics of schizophrenia, Augustin, New York.

732. KallmannF.J. (1946). The genetic theory of schizophrenia. An analysis of 691 schizophrénie twin index families, Am. J. Psychiatry, 103, 3.

733. Kan Y. W., Dozy A. M. (1978). Antenatal diagnosis of sicklecell anaemia by DNA analysis of amnioticfluid cells, Lancet, II, 910-912.

734. Kanneil W.B. (1976). Some lessons in cardiovascular epidemiolog from Framingham, Am. J. Cardiol, 37, 268-282.

735. KeatsB.J.B., Morton N. E., Rao D.C., Williams W. (1979). A sourse book for linkage in man, Johns Hopkins Univ. Press, Baltimore.

736. Keats J. В., Morton N. E., Rao D. C. (1981). Reduction of physical assigment to a standard lod table: Chromosome 1, Hum. Genet., 56, 353 359.

737. Kelley W.N., Greene M.L., Rosenbloom P.M., Henderson J.F., Seeqmiller J.E. (1969). Hypoxanthine-guanine phosphoribosyltranspherase deficiency in guut, Ann. Intern. Med., 70, 155.

IIS. Kiekebusch-Müller B.D., Arnold H., Mayr W. R. (1980). Ein Algorithmus zur Berechnung der HLA-Haplotypfrequenzen (an algorhithm for calculating HLA haplotype frequencies), Anthrop. Anzeiger, 38, 1-10.

739. Kissmeyer-Nielsen F. (ed.) (1975). Histocom-

patibility testing 1975, Munkagaard, Copenhagen.

740. Klein J. (1974). Genetic polymorphism of the histocompatibility 2 loci of the mouse, Ann. Rev. Genet., 8, 63-77.

741. Klein J. (1975). Biology of the mouse histocompatibility-2 complex, Springer, Berlin, Heidelberg, New York.

742. Kloimwieder R. (1942). Die Intelligenz in ihren Beziehungen zur Vererbung, Umwelt Übung, Z. Menschl. Vererbungs-Konstitutionslehre, 25, 582-617.

743. Knowler W. C., Pettit D.J., Vasquez B., Rotwein P. S. Andreone T. L., Permutt M. A. (1984). Polymorphism in the У flanking region of the human insulin gene, J. Clin. Invest., 74, 2129-2135.

744. Koller S. (1940). Methodik der menschlichen Erbforschung II. Die Erbstatistik in der Familie. 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. 261284.

Дата добавления: 2015-12-16 | Просмотры: 590 | Нарушение авторских прав