Improved diagnosis of a common mutation (R248C) in the human growth factor receptor 3 (FGFR3) gene that causes type I Thanatophoric dysplasia
Mehmet Simsek, Lihadh Al-Gazali, Reyhanah Al-Mjeni, Riad BayoumiVolume:
36
Year:
2003
Language:
english
Pages:
3
DOI:
10.1016/s0009-9120(02)00441-1
File:
PDF, 62 KB
english, 2003