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Two common mutations 934C to G and 937C to G of fibroblast growth factor receptor 2 (FGFR2) gene in Chinese patients with apert syndrome
Author(s) -
Tsai FuuJen,
Hwu WuhLiang,
Lin ShuanPei,
Chang JanGowth,
Wang TsoRen,
Tsai ChangHai
Publication year - 1998
Publication title -
human mutation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.981
H-Index - 162
eISSN - 1098-1004
pISSN - 1059-7794
DOI - 10.1002/humu.1380110106
Subject(s) - china , medicine , pediatrics , family medicine , history , archaeology