مرکز منطقه ای اطلاع رساني علوم و فناوري - Improved diagnosis of a common mutation (R248C) in the human growth factor receptor 3 (FGFR3) gene that causes type I Thanatophoric dysplasia

Title of article :

Improved diagnosis of a common mutation (R248C) in the human growth factor receptor 3 (FGFR3) gene that causes type I Thanatophoric dysplasia

Author/Authors :

Mehmet Simsek، نويسنده , , Lihadh Al Gazali، نويسنده , , Reyhanah Al-Mjeni، نويسنده , , Riad Bayoumi، نويسنده ,

Issue Information :

روزنامه با شماره پیاپی سال 2003

Pages :

From page :

151

To page :

153

Journal title :

Clinical Biochemistry

Serial Year :

2003

Journal title :

Clinical Biochemistry

Record number :

482386

Link To Document :