Paternal Origin of FGFR2 Mutations in Sporadic Cases of Crouzon Syndrome and Pfeiffer Syndrome
Authors:
- Wen JiangWen Jiang
- Simeon A. BoyadjievSBSimeon A. Boyadjiev
- Alissa K. TranATAlissa K. Tran
- Andrea A. ZacharyAZAndrea A. Zachary
- Lionel Van MaldergemLionel Van Maldergem
- David JohnsonDavid Johnson
- Sinead WalshSWSinead Walsh
- Michael OldridgeMOMichael Oldridge
- Steven A. WallSWSteven A. Wall
- Andrew O.M. WilkieAndrew O.M. Wilkie
- Ethylin Wang JabsEthylin Wang Jabs
Open Access
- 1 March 2000
- journal article
- Published by Elsevier in The American Journal of Human Genetics
- Vol. 66 (3) , 768-777
Abstract
No abstract availableKeywords
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