Paternal Origin of FGFR2 Mutations in Sporadic Cases of Crouzon Syndrome and Pfeiffer Syndrome
Open Access
- 1 March 2000
- journal article
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 66 (3), 768-777
- https://doi.org/10.1086/302831
Abstract
No abstract availableKeywords
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