No association betweenDFNA6 and Pro250Arg mutation inFGFR3
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference5 articles.
1. Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromes
2. Skeletal overgrowth and deafness in mice lacking fibroblast growth factor receptor 3
3. Deafness due to Pro250Arg mutation of FGFR3
4. A gene for autosomal dominant nonsyndromic hereditary hearing impairment maps to 4p16.3
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Muenke syndrome (FGFR3-related craniosynostosis): Expansion of the phenotype and review of the literature;American Journal of Medical Genetics Part A;2007
2. Syndrome of coronal craniosynostosis, Klippel-Feil anomaly, and sprengel shoulder with and without Pro250Arg mutation in the FGFR3 gene;American Journal of Medical Genetics;2001
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