Results 1 -
10
of
23
for
"Deafness," autosomal dominant 15
- ... RECESSIVE 13; DFNB13 DEAFNESS, AUTOSOMAL RECESSIVE 17; DFNB17 DEAFNESS, AUTOSOMAL DOMINANT 15; DFNA15 DEAFNESS, AUTOSOMAL RECESSIVE 18A; DFNB18A DEAFNESS, AUTOSOMAL ...
- ... Strom TM, Mignot E. Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy. Hum Mol Genet. 2012 May 15;21(10):2205-10. doi: 10.1093/hmg/ ...
- ... Strom TM, Mignot E. Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy. Hum Mol Genet. 2012 May 15;21(10):2205-10. doi: 10.1093/hmg/ ...
- ... gamma 1 actin-like protein cytoskeletal gamma-actin deafness, autosomal dominant 20 deafness, autosomal dominant 26 DFNA20 DFNA26 gamma-actin Tests of ACTG1 ...
- ... locus. Am J Med Genet A. 2007 Jul 15;143A(14):1623-9. doi: ... autosomal dominant, postlingual, progressive, mid frequency hearing loss in a ...
- The GJB3 gene provides instructions for making a protein called gap junction beta 3, more commonly known as connexin 31. This protein is part of the connexin ...
- ... DOMINANT; MYP12 MYOPIA 16, AUTOSOMAL DOMINANT; MYP16 MYOPIA 15, AUTOSOMAL DOMINANT; MYP15 MYOPIA 20, AUTOSOMAL DOMINANT; MYP20 MYOPIA 19, ...
- ... National Organization for Rare Disorders (NORD) KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT; KIDAD KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL RECESSIVE; KIDAR ...
- ... bones, nerve tissue, and muscles seen in craniofacial-deafness-hand syndrome. PAX3 This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ...
- ... Organization for Rare Disorders (NORD) KERATODERMA, PALMOPLANTAR, WITH DEAFNESS PubMed Birkenhager R, Lublinghoff N, Prera E, Schild C, Aschendorff A, Arndt S. Autosomal dominant prelingual hearing loss with palmoplantar keratoderma syndrome: Variability ...
