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Journal Abstract Search

124 related items for PubMed ID: 19159392

  • 1. A novel autosomal dominant deafness locus (DFNA58) maps to 2p12-p21.
    Lezirovitz K, Braga MC, Thiele-Aguiar RS, Auricchio MT, Pearson PL, Otto PA, Mingroni-Netto RC.
    Clin Genet; 2009 May; 75(5):490-3. PubMed ID: 19159392
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  • 3. Mapping of a new autosomal dominant non-syndromic hearing loss locus (DFNA43) to chromosome 2p12.
    Flex E, Mangino M, Mazzoli M, Martini A, Migliosi V, Colosimo A, Mingarelli R, Pizzuti A, Dallapiccola B.
    J Med Genet; 2003 Apr; 40(4):278-81. PubMed ID: 12676899
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  • 4. [Exclusive identification of gene loci of autosomal dominant nonsyndromic hearing loss].
    Wang Z, Wang S, Zhang B, Cui Y, Shen F, Hu Y.
    Lin Chuang Er Bi Yan Hou Ke Za Zhi; 2002 Apr; 16(4):147-9. PubMed ID: 12608274
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  • 8. A novel locus (DFNA24) for prelingual nonprogressive autosomal dominant nonsyndromic hearing loss maps to 4q35-qter in a large Swiss German kindred.
    Häfner FM, Salam AA, Linder TE, Balmer D, Baumer A, Schinzel AA, Spillmann T, Leal SM.
    Am J Hum Genet; 2000 Apr; 66(4):1437-42. PubMed ID: 10739769
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  • 12. DFNB93, a novel locus for autosomal recessive moderate-to-severe hearing impairment.
    Tabatabaiefar MA, Alasti F, Shariati L, Farrokhi E, Fransen E, Nooridaloii MR, Chaleshtori MH, Van Camp G.
    Clin Genet; 2011 Jun; 79(6):594-8. PubMed ID: 21542834
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  • 13. A new locus for dominant hereditary spastic paraplegia maps to chromosome 2p12.
    Züchner S, Kail ME, Nance MA, Gaskell PC, Svenson IK, Marchuk DA, Pericak-Vance MA, Ashley-Koch AE.
    Neurogenetics; 2006 May; 7(2):127-9. PubMed ID: 16565863
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  • 16. Sex-linked deafness.
    Petersen MB, Wang Q, Willems PJ.
    Clin Genet; 2008 Jan; 73(1):14-23. PubMed ID: 18005182
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  • 19. A locus for autosomal dominant keratoconus maps to human chromosome 3p14-q13.
    Brancati F, Valente EM, Sarkozy A, Fehèr J, Castori M, Del Duca P, Mingarelli R, Pizzuti A, Dallapiccola B.
    J Med Genet; 2004 Mar; 41(3):188-92. PubMed ID: 14985379
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  • 20. Gingival fibromatosis with sensorineural hearing loss: an autosomal dominant trait.
    Hartsfield JK, Bixler D, Hazen RH.
    Am J Med Genet; 1985 Nov; 22(3):623-7. PubMed ID: 4061496
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