Non-syndromic progressive hearing loss DFNA38 is caused by heterozygous missense mutation in the Wolfram syndrome gene WFS1

By Griffin A.  

Human Molecular Genetics, Vol. 10, Iss. 22, 2001-10 ,pp. : 2509-2514

Oxford University Press

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A novel missense mutation in the paired domain of PAX9 causes non-syndromic oligodontia

By Jumlongras Dolrudee   Lin Jenn-Yih   Chapra Anas   Seidman Christine   Seidman Jonathan   Maas Richard   Olsen Bjorn  

Human Genetics, Vol. 114, Iss. 3, 2004-02 ,pp. : 242-249

Springer Publishing Company

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A Gene for Non-Syndromic Autosomal Dominant Progressive Postlingual Sensorineural Hearing Loss Maps to Chromosome 14q12–13

By Manolis Evangelos N.  

Human Molecular Genetics, Vol. 5, Iss. 7, 1996-01 ,pp. : 1047-1050

Oxford University Press

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A Gene for Autosomal Dominant Late-Onset Progressive Non-Syndromic Hearing Loss, DFNA10 , Maps to Chromosome 6

By O'Neill Marsha E.   Marietta Jacquie   Nishimura Darryl   Wayne Sigrid   Van Camp Guy   Van Laer Lut   Negrini Clelia   Wilcox Edward R.   Chen Achih   Fukushima Kunihiro   Ni Li   Sheffield Val C.   Smith Richard J. H.  

Human Molecular Genetics, Vol. 5, Iss. 6, 1996-01 ,pp. : 853-856

Oxford University Press

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Biochemical Evidence for Nuclear Gene Involvement in Phenotype of Non-Syndromic Deafness Associated with Mitochondrial 12S rRNA Mutation

By Guan Min-Xin   Fischel-Ghodsian Nathan   Attardi Giuseppe  

Human Molecular Genetics, Vol. 5, Iss. 7, 1996-01 ,pp. : 963-971

Oxford University Press

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