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Syndromes / Congenital disorders / Skull / Genodermatoses / Craniosynostosis / Apert syndrome / Fibroblast growth factor receptor 2 / Saethre-Chotzen syndrome / Suture / Health / Anatomy / Human anatomy


DEVELOPMENTAL DYNAMICS 239:3058–3071, 2010 a PATTERNS & PHENOTYPES
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Document Date: 2010-10-27 13:48:41


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Park / Generalitat de Catalunya / FGFR2 S252W / New York / /

Company

BP / Ford / C 2010 Wiley-Liss Inc. / V 2010 Wiley-Liss Inc. C / /

Country

Columbia / Spain / /

Currency

pence / /

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Facility

University of Missouri-School / Pennsylvania State University / Wiley Online Library / University Park / /

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http /

MedicalCondition

Bicoronal synostosis / partial synostosis / Apert syndrome / disease / partial and unicoronal synostosis / Apert syndrome FGFR2 / related genetic disorders / INTRODUCTION Apert syndrome / proptosis / congenital autosomal dominant disorder / coronal synostosis / Fgfr2þ/P253R Apert syndrome / cleft palate / Muenke craniosynostosis syndrome / Joan T. Richtsmeier1* Apert syndrome / unicoronal synostosis / congenital disorder / synostosis / plasia / ocular hypertelorism / related craniosynostosis / Apert syndrome Fgfr2þ/S252W / craniosynostosis / /

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Department of Pathology & Anatomical Sciences / National Institute of Health / School of Medicine / Mount Sinai School of Medicine / Pennsylvania State University / University of Missouri / Department of Genetics and Genomic Sciences / Department of Anthropology / /

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Joan T. Richtsmeier / Gustave L. Levy / /

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developing head / General / Carpenter / /

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Missouri / Alabama / Pennsylvania / New York / /

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tomography / gene expression / cell signaling / genotype / html / /

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http /

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