Deafness due to Pro250Arg mutation of FGFR3.

Hollway, G E

Deafness due to Pro250Arg mutation of FGFR3. [electronic resource] - Lancet (London, England) Mar 1998 - 877-8 p. digital

Publication Type: Letter; Research Support, Non-U.S. Gov't

0140-6736

10.1016/S0140-6736(98)24012-8 doi


Craniosynostoses--complications
Deafness--genetics
Hearing Loss, Sensorineural--complications
Humans
Pedigree
Point Mutation
Receptors, Fibroblast Growth Factor--genetics