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Journal Abstract Search

90 related items for PubMed ID: 12788910

  • 1. A locus for autosomal recessive idiopathic hypogonadotropic hypogonadism on chromosome 19p13.3.
    Acierno JS, Shagoury JK, Bo-Abbas Y, Crowley WF, Seminara SB.
    J Clin Endocrinol Metab; 2003 Jun; 88(6):2947-50. PubMed ID: 12788910
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  • 2. DFNB68, a novel autosomal recessive non-syndromic hearing impairment locus at chromosomal region 19p13.2.
    Santos RL, Hassan MJ, Sikandar S, Lee K, Ali G, Martin PE, Wambangco MA, Ahmad W, Leal SM.
    Hum Genet; 2006 Aug; 120(1):85-92. PubMed ID: 16703383
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  • 3. A new locus for autosomal recessive nuclear cataract mapped to chromosome 19q13 in a Pakistani family.
    Riazuddin SA, Yasmeen A, Zhang Q, Yao W, Sabar MF, Ahmed Z, Riazuddin S, Hejtmancik JF.
    Invest Ophthalmol Vis Sci; 2005 Feb; 46(2):623-6. PubMed ID: 15671291
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  • 5. Autosomal recessive idiopathic hypogonadotropic hypogonadism: genetic analysis excludes mutations in the gonadotropin-releasing hormone (GnRH) and GnRH receptor genes.
    Bo-Abbas Y, Acierno JS, Shagoury JK, Crowley WF, Seminara SB.
    J Clin Endocrinol Metab; 2003 Jun; 88(6):2730-7. PubMed ID: 12788881
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  • 6. Fine mapping of a locus for nonsyndromic mental retardation on chromosome 19p13.
    Nolan DK, Chen P, Das S, Ober C, Waggoner D.
    Am J Med Genet A; 2008 Jun 01; 146A(11):1414-22. PubMed ID: 18446860
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  • 12. A novel locus for restless legs syndrome maps to chromosome 19p in an Irish pedigree.
    Skehan EB, Abdulrahim MM, Parfrey NA, Hand CK.
    Neurogenetics; 2012 May 01; 13(2):125-32. PubMed ID: 22411506
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  • 16. Linkage of Bardet-Biedl syndrome to chromosome 16q and evidence for non-allelic genetic heterogeneity.
    Kwitek-Black AE, Carmi R, Duyk GM, Buetow KH, Elbedour K, Parvari R, Yandava CN, Stone EM, Sheffield VC.
    Nat Genet; 1993 Dec 01; 5(4):392-6. PubMed ID: 8298649
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  • 19. [A new locus for an autosomal dominant, non-syndromic hearing impairment (DFNA57) located on chromosome 19p13.2 and overlapping with DFNB15].
    Bönsch D, Schmidt CM, Scheer P, Bohlender J, Neumann C, am Zehnhoff-Dinnesen A, Deufel T.
    HNO; 2008 Feb 01; 56(2):177-82. PubMed ID: 18066515
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