A novel autosomal recessive non-syndromic deafness locus (DFNB35) maps to 14q24.1–14q24.3 in large consanguineous kindred from Pakistan-Reference-Cited by-同舟云学术

A novel autosomal recessive non-syndromic deafness locus (DFNB35) maps to 14q24.1–14q24.3 in large consanguineous kindred from Pakistan

Published:2003-01 Issue:1 Volume:11 Page:77-80
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Ansar Muhammad,Din Mohammad Amin ud,Arshad Muhammad,Sohail Muhammad,Faiyaz-Ul-Haque Mohammad,Haque Sayedul,Ahmad Wasim,Leal Suzanne M

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/5200905.pdf

Reference14 articles.

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2. Bergstrom L, Hemenway WG & Downs MP : A high risk registry to find congenital deafness. Otolaryngol Clin North Am 1971; 4: 369–399.

3. Van Camp G, Willems PJ & Smith RJH : Nonsyndromic hearing impairment: unparalleled heterogeneity. Am J Hum Genet 1997; 60: 758–764.

4. Van Camp G & Smith RJH : Hereditary Hearing Loss Homepage. URL: http://dnalab-www.uia.ac.be/dnalab/hhh/, August 2002.

5. Cohen M & Gorlin R : Epidemiology, etiology, and genetic patterns. in: Gorlin R, Toriello H, Cohen M (eds): Hereditary Hearing Loss and its Syndromes, Oxford: Oxford University Press. 1995. pp 9–21.

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