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FGFR2 mutation in a Chinese family with unusual Crouzon syndrome

Zi-Li Li1, Xue Chen2, Wen-Juan Zhuang1

  • 1Ningxia Eye Hospital, People Hospital of Ningxia Hui Autonomous Region (First Affiliated Hospital of Northwest University for Nationalities), Yinchuan 750001, Ningxia Hui Autonomous Region, China.

International Journal of Ophthalmology
|November 3, 2016
PubMed
Abstract

Keywords:
Crouzon syndromeFGFR2 mutationfamilial casesphenotypic diversity

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