Noggin heterozygous mice: an animal model for congenital conductive hearing loss in humans
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics (clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/article-pdf/17/6/844/17245957/ddm356.pdf
Reference42 articles.
1. Heterozygous mutations in the gene encoding noggin affect human joint morphogenesis;Gong;Nat. Genet.,1999
2. Autosomal dominant stapes ankylosis with broad thumbs and toes, hyperopia, and skeletal anomalies is caused by heterozygous nonsense and frameshift mutations in NOG, the gene encoding noggin;Brown;Am. J. Hum. Genet.,2002
3. Identical mutations in NOG can cause either tarsal/carpal coalition syndrome or proximal symphalangism;Dixon;Genet. Med.,2001
4. Teunissen–Cremers syndrome: a clinical, surgical, and genetic report;Weekamp;Otol. Neurotol.,2005
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