Pfeiffer syndrome with FGFR2 W290C mutation perinatally presenting extreme proptosis

Pfeiffer syndrome with FGFR2 W290C mutation perinatally presenting extreme proptosis

Bibliographic Details
Main Authors:	Chih-Ping Chen, Hsu-Kuang Huang, Yu-Peng Liu, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang
Format:	Article
Language:	English
Published:	Elsevier 2013-12-01
Series:	Taiwanese Journal of Obstetrics & Gynecology
Online Access:	http://www.sciencedirect.com/science/article/pii/S1028455913001940

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