A Novel Locus for Non-syndromic Sensorineural Deafness ( DFN6 ) Maps to Chromosome Xp22

By del Castillo Ignacio   Villamar Manuela   Sarduy Maritza   Romero Lourdes   Herraiz Carlos   Javier Hernández F.   Rodríguez Mariano   Borrás Isabel   Montero Ángeles   Bellón Joaquín   Cruz Tapia M.   Moreno Felipe  

Human Molecular Genetics, Vol. 5, Iss. 9, 1996-01 ,pp. : 1383-1387

Oxford University Press

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A Gene Responsible for a Sensorineural Nonsyndromic Recessive Deafness Maps to Chromosome 2p22–23

By Chaïb Hassan   Place Christophe   Salem Nabiha   Chardenoux Sébastien   Vincent Christophe   Weissenbach Jean   El-Zir Elie   Loiselet Jacques   Petit Christine  

Human Molecular Genetics, Vol. 5, Iss. 1, 1996-01 ,pp. : 155-158

Oxford University Press

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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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An α-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21

By Mustapha M.  

Human Molecular Genetics, Vol. 8, Iss. 3, 1999-03 ,pp. : 409-412

Oxford University Press

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Two Different Connexin 26 Mutations in an Inbred Kindred Segregating Non-Syndromic Recessive Deafness: Implications for Genetic Studies in Isolated Populations

By Carrasquillo Minerva M.   Zlotogora Joel   Barges Saleh   Chakravarti Aravinda  

Human Molecular Genetics, Vol. 6, Iss. 12, 1997-11 ,pp. : 2163-2172

Oxford University Press

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