FGFR2 mutation in a patient with Apert syndrome associated...

Congenital Anomalies 2003 Vol. 43; Iss. 4

FGFR2 mutation in a patient with Apert syndrome associated with humeroradial synostosis

Yumiko Kanauchi, Yasuteru Muragaki, Toshihiko Ogino, Masatoshi Takahara, Hiroyuki Tsuchida, Daisuke Ishigaki
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Volume:
43
Year:
2003
Language:
english
Pages:
4
DOI:
10.1111/j.1741-4520.2003.tb01017.x
File:
PDF, 398 KB
english, 2003
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