Deafness due to Pro250Arg mutation of FGFR3
- 1 March 1998
- journal article
- Published by Elsevier in The Lancet
- Vol. 351 (9106) , 877-878
- https://doi.org/10.1016/s0140-6736(98)24012-8
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- Prevalence of Pro250Arg mutation of fibroblast growth factor receptor 3 in coronal craniosynostosisThe Lancet, 1997
- Skeletal overgrowth and deafness in mice lacking fibroblast growth factor receptor 3Nature Genetics, 1996
- A gene for autosomal dominant nonsyndromic hereditary hearing impairment maps to 4p16.3Human Molecular Genetics, 1995
- Fibroblast-growth-factor receptor mutations in human skeletal disordersTrends in Genetics, 1995