Improved diagnosis of a common mutation (R248C) in the...

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 Bayoumi
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Volume:
36
Year:
2003
Language:
english
Pages:
3
DOI:
10.1016/s0009-9120(02)00441-1
File:
PDF, 62 KB
english, 2003
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