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Journal Abstract Search

124 related items for PubMed ID: 8209924

  • 21. Infantile lethal variant of Simpson-Golabi-Behmel syndrome associated with hydrops fetalis.
    Terespolsky D, Farrell SA, Siegel-Bartelt J, Weksberg R.
    Am J Med Genet; 1995 Nov 20; 59(3):329-33. PubMed ID: 8599356
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  • 24. Tentative assignment of gene for oto-palato-digital syndrome to distal Xq (Xq26-q28).
    Hoar DI, Field LL, Beards F, Hoganson G, Rollnick B, Hoo JJ.
    Am J Med Genet; 1992 Jan 15; 42(2):170-2. PubMed ID: 1733165
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  • 25. GPC4, the gene for human K-glypican, flanks GPC3 on xq26: deletion of the GPC3-GPC4 gene cluster in one family with Simpson-Golabi-Behmel syndrome.
    Veugelers M, Vermeesch J, Watanabe K, Yamaguchi Y, Marynen P, David G.
    Genomics; 1998 Oct 01; 53(1):1-11. PubMed ID: 9787072
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  • 26. The autosomal recessive Kenny-Caffey syndrome locus maps to chromosome 1q42-q43.
    Diaz GA, Khan KT, Gelb BD.
    Genomics; 1998 Nov 15; 54(1):13-8. PubMed ID: 9806825
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  • 27. Simpson-Golabi-Behmel syndrome and attention deficit hyperactivity disorder in two brothers.
    Savarirayan R, Bankier A.
    J Med Genet; 1999 Jul 15; 36(7):574-6. PubMed ID: 10424824
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  • 28. Simpson-Golabi-Behmel syndrome: an X-linked encephalo-tropho-schisis syndrome.
    Neri G, Marini R, Cappa M, Borrelli P, Opitz JM.
    Am J Med Genet; 1988 Jul 15; 30(1-2):287-99. PubMed ID: 3177455
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  • 29. Linkage of the gene for an X-linked mental retardation disorder to a hypervariable (AGAT)n repeat motif within the human hypoxanthine phosphoribosyltransferase (HPRT) locus (Xq26).
    Huang TH, Hejtmancik JF, Edwards A, Pettigrew AL, Herrera CA, Hammond HA, Caskey CT, Zoghbi HY, Ledbetter DH.
    Am J Hum Genet; 1991 Dec 15; 49(6):1312-9. PubMed ID: 1746558
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  • 32. Homozygosity mapping of a Weill-Marchesani syndrome locus to chromosome 19p13.3-p13.2.
    Faivre L, Mégarbané A, Alswaid A, Zylberberg L, Aldohayan N, Campos-Xavier B, Bacq D, Legeai-Mallet L, Bonaventure J, Munnich A, Cormier-Daire V.
    Hum Genet; 2002 Apr 15; 110(4):366-70. PubMed ID: 11941487
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  • 34. Genetic localisation of MRX27 to Xq24-26 defines another discrete gene for non-specific X-linked mental retardation.
    Gedeon AK, Glass IA, Connor JM, Mulley JC.
    Am J Med Genet; 1996 Jul 12; 64(1):121-4. PubMed ID: 8826461
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  • 39. Recombination between the factor VIII gene and the DXS52 locus gives the most probable genetic order as centromere-fra(X)-DXS15-DXS52-F8C-telomere.
    Mulligan LM, Grover HJ, Blanchette VS, Giles AR, Lillicrap DP, Phillips A, Holden JJ, White BN.
    Am J Med Genet; 1987 Mar 12; 26(3):751-60. PubMed ID: 3105317
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