A Gene for a Dominant Form of Non-Syndromic Sensorineural Deafness ( DFNA11 ) Maps Within the Region Containing the DFNB2 Recessive Deafness Gene

By Tamagawa Yuya   Kitamura Ken   Ishida Takashi   Ishikawa Kazuhiro   Tanaka Hajime   Tsuji Shoji   Nishizawa Masatoyo  

Human Molecular Genetics, Vol. 5, Iss. 6, 1996-01 ,pp. : 849-852

Oxford University Press

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Connexin26 Mutations Associated with the Most Common Form of Non-Syndromic Neurosensory Autosomal Recessive Deafness (DFNB1) in Mediterraneans

By Zelante Leopoldo   Gasparini Paolo   Estivill Xavier  

Human Molecular Genetics, Vol. 6, Iss. 9, 1997-01 ,pp. : 1605-1609

Oxford University Press

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Autosomal Recessive Non-Syndromic Deafness Locus (DFNB8) Maps on Chromosome 21Q22 in a Large Consanguineous Kindred from Pakistan

By Veske Andres   Oehlmann Ralph   Younus Farah   Mohyuddin Aisha   Müller-Myhsok Bertram   Qasim Mehdi S.   Gal Andreas  

Human Molecular Genetics, Vol. 5, Iss. 1, 1996-01 ,pp. : 165-168

Oxford University Press

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A Novel Autosomal Recessive Non-Syndromic Deafness Locus, DFNB66, Maps to Chromosome 6p21.2-22.3 in a Large Tunisian Consanguineous Family

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Human Heredity, Vol. 60, Iss. 3, 2006-01 ,pp. : 123-128

Karger

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Mapping of DFNB12 , a Gene for a Non-Syndromal Autosomal Recessive Deafness, to Chromosome 10q21–22

By Chaïb Hassan  

Human Molecular Genetics, Vol. 5, Iss. 7, 1996-01 ,pp. : 1061-1064

Oxford University Press

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