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A novel mutation in the MSX2 gene in a family with foramina parietalia permagna (FPP)

✍ Scribed by Liesbeth Spruijt; Pieter Verdyck; Wim Van Hul; Wim Wuyts; Christine de Die-Smulders

Publisher: John Wiley and Sons
Year: 2005
Tongue: English
Weight: 94 KB
Volume: 139A
Category: Article
ISSN: 1552-4825
DOI: 10.1002/ajmg.a.30923

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