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Journal Abstract Search

155 related items for PubMed ID: 1674730

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  • 26. Exclusion mapping of 12 X-linked disease loci and 10 DNA probes from the long arm of the X-chromosome.
    Yang HM, Lund T, Niebuhr E, Nørby S, Schwartz M, Shen L.
    Clin Genet; 1990 Aug; 38(2):94-104. PubMed ID: 1976460
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  • 27. No genetic linkage detected for schizophrenia to Xq27-q28.
    Delisi LE, Crow TJ, Davies KE, Terwilliger JD, Ott J, Ram R, Flint T, Boccio A.
    Br J Psychiatry; 1991 May; 158():630-4. PubMed ID: 1677599
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  • 28. Linkage and genetic counselling for the fragile X using DNA probes 52A, F9, DX13, and ST14.
    Mulley JC, Gedeon AK, Thorn KA, Bates LJ, Sutherland GR.
    Am J Med Genet; 1987 Jun; 27(2):435-48. PubMed ID: 2886048
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  • 29. Linkage analysis in the fragile X syndrome using multiple distal Xq polymorphic DNA markers.
    Glass IA, Pirrit LA, White EM, Bell MV, Davies KE, Cockburn F, Connor JM.
    Am J Med Genet; 1991 Jun; 38(2-3):298-304. PubMed ID: 1673301
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  • 30. Analysis of fragile X-mental retardation families using flanking polymorphic DNA probes.
    Goonewardena P, Gustavson KH, Holmgren G, Tolun A, Chotai J, Johnsen E, Pettersson U.
    Clin Genet; 1986 Oct; 30(4):249-54. PubMed ID: 2878749
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  • 31. The gene for X-linked hydrocephalus maps to Xq28, distal to DXS52.
    Lyonnet S, Pelet A, Royer G, Delrieu O, Serville F, le Marec B, Gruensteudel A, Pfeiffer RA, Briard ML, Dubay C.
    Genomics; 1992 Oct; 14(2):508-10. PubMed ID: 1427869
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  • 34. Emery-Dreifuss muscular dystrophy: linkage to markers in distal Xq28.
    Yates JR, Warner JP, Smith JA, Deymeer F, Azulay JP, Hausmanowa-Petrusewicz I, Zaremba J, Borkowska J, Affara NA, Ferguson-Smith MA.
    J Med Genet; 1993 Feb; 30(2):108-11. PubMed ID: 8445613
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  • 36. Mapping of a gene for non-specific X linked mental retardation: evidence for linkage to chromosomal region Xp21.1-Xp22.3.
    Kozák L, Chiurazzi P, Genuardi M, Pomponi MG, Zollino M, Neri G.
    J Med Genet; 1993 Oct; 30(10):866-9. PubMed ID: 8230164
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  • 38. A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22.
    Tranebjaerg L, Schwartz C, Eriksen H, Andreasson S, Ponjavic V, Dahl A, Stevenson RE, May M, Arena F, Barker D.
    J Med Genet; 1995 Apr; 32(4):257-63. PubMed ID: 7643352
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  • 39. Physical and genetic mapping of polymorphic loci in Xq28 (DXS15, DXS52, and DXS134): analysis of a cosmid clone and a yeast artificial chromosome.
    Feil R, Palmieri G, d'Urso M, Heilig R, Oberlé I, Mandel JL.
    Am J Hum Genet; 1990 Apr; 46(4):720-8. PubMed ID: 1969226
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