FGFR2 mutation and genotype-phenotype analysis in eight...

Congenital Anomalies 2000 Vol. 40; Iss. 4

FGFR2 mutation and genotype-phenotype analysis in eight Japanese patients associated with Apert syndrome

Mail Tsukuno, Hideaki Suzuki, Kunitoshi Ninomiya, Yoshikatsu Eto, Kunihiro Kurihara
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Volume:
40
Year:
2000
Language:
english
Pages:
5
DOI:
10.1111/j.1741-4520.2000.tb00926.x
File:
PDF, 512 KB
english, 2000
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