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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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  

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Springer Publishing Company

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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

Karger

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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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DFNB44, a Novel Autosomal Recessive Non-Syndromic Hearing Impairment Locus, Maps to Chromosome 7p14.1-q11.22

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