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

European Journal of Human Genetics

Volumn 11, Issue 1, 2003, Pages 77-80

  Ansar, Muhammad ^a   Amin ud Din, Mohammad ^b   Arshad, Muhammad ^a   Sohail, Muhammad ^c   Faiyaz Ul Haque, Mohammad ^d   Haque, Sayedul ^a   Ahmad, Wasim ^a   Leal, Suzanne M ^e  

^a QUAID I AZAM UNIVERSITY   (Pakistan)

^b GC UNIVERSITY   (Pakistan)

^c UNIVERSITY OF OXFORD   (United Kingdom)

^d HOSPITAL FOR SICK CHILDREN   (Canada)

^e BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

14q24.1 14q24.3 prelingual; Autosomal recessive nonsyndromic hearing loss; DFNA23; DFNA9; DFNB35; DFNB5; Pakistan

Indexed keywords

DNA;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHROMOSOME 14Q; CHROMOSOME MAP; CLINICAL ARTICLE; CLINICAL FEATURE; CONSANGUINITY; CONTROLLED STUDY; DISEASE SEVERITY; FAMILY; FEMALE; GENE ISOLATION; GENE LOCUS; GENETIC MARKER; GENETIC SCREENING; HAPLOTYPE; HEARING IMPAIRMENT; HOMOZYGOSITY; HUMAN; LINKAGE ANALYSIS; MALE; PAKISTAN; PHENOTYPE; PRIORITY JOURNAL; SCORING SYSTEM;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 14; CONSANGUINITY; DEAFNESS; FEMALE; GENES, RECESSIVE; GENETIC MARKERS; HOMOZYGOTE; HUMANS; LINKAGE (GENETICS); LOD SCORE; MALE; PAKISTAN; PEDIGREE; RECOMBINATION, GENETIC;

EID: 0037265540     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5200905     Document Type: Article

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