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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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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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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Linkage Studies of Non-Syndromic Recessive Deafness (NSRD) in a Family Originating from the Mirpur Region of Pakistan Maps DFNB1 Centromeric to D13S175

By Brown K. A.   Janjua A. H.   Karbani G.   Parry G.   Noble A.   Crockford G.   Bishop D. T.   Newton V. E.   Markham A. F.   Mueller R. F.  

Human Molecular Genetics, Vol. 5, Iss. 1, 1996-01 ,pp. : 169-173

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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