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Article

Pfeiffer syndrome with FGFR2 W290C mutation perinatally presenting extreme proptosis.

Taiwanese journal of obstetrics & gynecology - 1 Dec 2013

Chen Chih-Ping, Huang Hsu-Kuang, Liu Yu-Peng, Chern Schu-Rern, Su Jun-Wei, Wang Wayseen

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Share to Acrocephalosyndactylia
Share to FGFR2 gene
Share to Infant, Newborn
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Receptor, Fibroblast Growth Factor, Type 2

Share to Ultrasonography, Prenatal

Source

Identifiers

PMID: 24411056
DOI: 10.1016/j.tjog.2013.10.031

Genes

FGFR2

Variants

Provenance

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