A second Middle Eastern kindred with autosomal recessive non-syndromic hearing loss segregates DFNB9

European Journal of Human Genetics

Volumn 6, Issue 4, 1998, Pages 341-344

  Leal, Suzanne M ^a,b,e   Apaydin, Fazil ^c   Barnwell, Carol ^d   Iber, Metin ^c   Kandogan, Tolga ^c   Pfister, Markus ^b   Braendle, Uwe ^b   Cura, Orhan ^c   Schwalb, Marvin ^d   Zenner, Hans Peter ^b   Vitale, Emilia ^d  

^a ROCKEFELLER UNIVERSITY   (United States)

^b UNIVERSITY OF TÜBINGEN   (Germany)

^c EGE UNIVERSITY SCHOOL OF MEDICINE   (Turkey)

^d RUTGERS NEW JERSEY MEDICAL SCHOOL   (United States)

^e Box 192   (United States)

Author keywords

Autosomal recessive non syndromic hearing loss; DFNB9; Sensorineural hearing loss

Indexed keywords

ARTICLE; CHROMOSOME 2P; CONGENITAL DEAFNESS; CONSANGUINITY; DATA BASE; GENE MAPPING; GENETIC LINKAGE; GENOTYPE; HUMAN; PRIORITY JOURNAL; TURKEY (REPUBLIC);

EID: 13144259710     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5200201     Document Type: Article

References (12)

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