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A novel KIF11 mutation in a Turkish patient with microcephaly, lymphedema, and chorioretinal dysplasia from a consanguineous family

✍ Scribed by Filiz Hazan; Pia Ostergaard; Taylan Ozturk; Esin Kantekin; Fusun Atlihan; Steve Jeffery; Ferda Ozkinay

Book ID: 111995197
Publisher: John Wiley and Sons
Year: 2012
Tongue: English
Weight: 132 KB
Volume: 158A
Category: Article
ISSN: 1552-4825
DOI: 10.1002/ajmg.a.35371

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