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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

144 related items for PubMed ID: 8652029

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  • 25. A novel locus for autosomal dominant nonsyndromic hearing loss, DFNA50, maps to chromosome 7q32 between the DFNB17 and DFNB13 deafness loci.
    Modamio-Høybjør S, Moreno-Pelayo MA, Mencía A, del Castillo I, Chardenoux S, Morais D, Lathrop M, Petit C, Moreno F.
    J Med Genet; 2004 Feb; 41(2):e14. PubMed ID: 14757864
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  • 35. [Modern concepts of the role of heredity in the origin of monosymptomatic hearing disorders in children].
    Bliumina MG, Moskovkina AG.
    Vestn Otorinolaringol; 1980 Feb; (1):67-73. PubMed ID: 6990581
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  • 38. Clinical and genetic features of nonsyndromic autosomal dominant sensorineural hearing loss: KCNQ4 is a gene responsible in Japanese.
    Akita J, Abe S, Shinkawa H, Kimberling WJ, Usami S.
    J Hum Genet; 2001 Feb; 46(7):355-61. PubMed ID: 11450843
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