Results 81 to 86 of about 139 (86)

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, 2003
Muahmmad Ansar, Muhammad Sohail, Wasim Ahmad   +2 more
exaly  

Mutations of MYO6 Are Associated with Recessive Deafness, DFNB37

American Journal of Human Genetics, 2003
Andrew J Griffith, Robert J. Morell, Zubair M Ahmed   +2 more
exaly  

Identification of a novel homozygous mutation in in a Chinese family with DFNB30 non-syndromic hearing impairment

International Journal of Pediatric Otorhinolaryngology, 2016
Li Jin, Ronggui Qu
exaly  

A mouse model for human hearing loss DFNB30 due to loss of function of myosin IIIA

Mammalian Genome, 2010
Mary-Claire King, Moien Kanaan, Karen Avraham   +2 more
exaly  

Functional pathogenicity of ESRRB variant of uncertain significance contributes to hearing loss (DFNB35)

Scientific Reports
Jae-Jin Song, Sang Yeon Lee, Won Hoon Choi   +2 more
exaly  

DFNB39

2018
exaly