Results 131 to 135 of about 12,592,373 (135)

Non‐syndromic, autosomal‐recessive deafness

Clinical Genetics, 2006
Michael Bjørn Petersen, Patrick J Willems   +1 more
exaly  

GJB2 c.−23+1G>A mutation is second most common mutation among Iranian individuals with autosomal recessive hearing loss

European Archives of Oto-Rhino-Laryngology, 2014
Leili Rejali, Sarah Azadmehr
exaly  

Novel CLDN14 mutations in Pakistani families with autosomal recessive non‐syndromic hearing loss

American Journal of Medical Genetics, Part A, 2012
Muahmmad Ansar, Kwanghyuk Lee, Bushra Khan   +2 more
exaly  

Novel TMPRSS3 variants in Pakistani families with autosomal recessive non‐syndromic hearing impairment

Clinical Genetics, 2012
Saadullah Khan, Muahmmad Ansar, Kwanghyuk Lee   +2 more
exaly  

Autosomal recessive non-syndromic hearing loss is caused by novel compound heterozygous mutations in TMC1 from a Tibetan Chinese family

International Journal of Pediatric Otorhinolaryngology, 2014
exaly