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

By  

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

Karger

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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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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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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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