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

✍ Scribed by Mail Tsukuno; Hideaki Suzuki; Kunitoshi Ninomiya; Yoshikatsu Eto; Kunihiro Kurihara

Book ID
111300690
Publisher
John Wiley and Sons
Year
2000
Tongue
English
Weight
512 KB
Volume
40
Category
Article
ISSN
0914-3505

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