Autosomal recessive nonsyndromic deafness locus DFNB63 at chromosome 11q13.2–q13.3

By Khan Shahid   Riazuddin Saima   Tariq Muhammad   Anwar Saima   Shabbir Muhammad   Riazuddin S.   Khan Shaheen   Husnain Tayyab   Ahmed Zubair   Friedman Thomas   Riazuddin Sheikh  

Human Genetics, Vol. 120, Iss. 6, 2007-02 ,pp. : 789-793

Springer Publishing Company

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

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

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

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

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

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

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