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Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome | Researchclopedia
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Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome
1995
929 citations
Journal Article
Field-Weighted Citation Impact:
35.89
University College London
David J. David
·
Women's and Children's Hospital
Louise J. Pulleyn
Paul Rutland
S Malcolm
Robin M. Winter
William Reardon