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

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

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

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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

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

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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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Localization of A Novel Autosomal Recessive Non-Syndromic Hearing Impairment Locus (DFNB38) to 6q26-q27 in a Consanguineous Kindred from Pakistan

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