1 | DFNA57, DFNB15
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| [A new locus for an autosomal dominant, non-syndromic hearing impairment (DFNA57) located on chromosome 19p13.2 and overlapping with DFNB15]
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| Bönsch D, Schmidt CM, Scheer P, Bohlender J, Neumann C, am Zehnhoff-Dinnesen A, Deufel T.
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| HNO 56(2):177-82. German.
2008
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2 | DFNA8, DFNB15, DM2
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| A novel locus for autosomal dominant, non-syndromic hearing impairment (DFNA18) maps to chromosome 3q22 immediately adjacent to the DM2 locus.
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| Bonsch D, Scheer P, Neumann C, Lang-Roth R, Seifert E, Storch P, Weiller C, Lamprecht-Dinnesen A, Deufel T.
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| Eur J Hum Genet 9(3):165-70. 2001
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3 | DFNB41, MYO1F, DFNB15
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| MYO1F as a candidate gene for nonsyndromic deafness, DFNB15.
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| Chen AH, Stephan DA, Hasson T, Fukushima K, Nelissen CM, Chen AF, Jun AI, Ramesh A, Van Camp G, Smith RJ.
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| Arch Otolaryngol Head Neck Surg 127(8):921-5. 2001
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4 | DFN2, DFNA10, DFNA13, DFNA18, DFNA2, DFNA4, DFNA5, DFNA6, DFNB12, DFNB13, DFNB15, DFNB16, DFNB17, DFNB19, DFNB6, DFNB7, DFNB8, USH1D, USH1E, USH1F, CLRN1
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| Human cochlear expressed sequence tags provide insight into cochlear gene expression and identify candidate genes for deafness.
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| Skvorak AB, et al.
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| Hum Mol Genet 8(3):439-52 1999
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5 | DFNB41, DFNB15
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| New gene for autosomal recessive non-syndromic hearing loss maps to either chromosome 3q or 19p.
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| Chen A, Wayne S, Bell A, Ramesh A, Srisailapathy CR, Scott DA, Sheffield VC, Van Hauwe P, Zbar RI, Ashley J, Lovett M, Van Camp G, Smith RJ.
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| Am J Med Genet 71(4):467-71. 1997
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