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Genodermatoses / Congenital disorders / Rare diseases / Craniofrontonasal syndrome / Cytogenetics / Crouzon syndrome / Pfeiffer syndrome / Apert syndrome / EFNB1 / Health / Syndromes / Genetics


Document Date: 2012-12-11 09:49:19

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City

Magdeburg / BRISTOL / New York / /

Company

Oxford University Press / RE (eds) Oxford University Press / nd Limited / /

Country

Germany / Canada / United Kingdom / /

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IndustryTerm

chemical change / affected carrier / /

MedicalCondition

nd Cleft lip / bicoronal synostosis / Craniofrontonasal syndrome / Frampton Cotterell Craniofrontonasal Syndrome / Apert Syndrome / cancer / syndactyly / red/green colour blindness / rarer craniosynostosis / nd Coronal craniosynostosis / present Cleft palate / craniofrontonasal dysostosis / Saethre-Chotzen Syndrome / heart disease / hypertelorism / diabetes / diaphragmatic hernia / Coronal craniosynostosis / Clinical Disorders / Pfeiffer Syndrome / cleft palate / unicoronal synostosis / Non-syndromic Craniosynostosis / Crouzon Syndrome / cleft lip / syndrome / Muenke Syndrome / Craniosynostosis / /

Organization

Oxford Craniofacial Unit / RF Twigg and Professor Andrew OM Wilkie Clinical Genetics Group Weatherall Institute / Oxford University / /

Person

Anthony Wynshaw-Boris / Robert P. Erickson / Michael Cohen / Charles J. Epstein / Gil Ruff / /

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Position

Professor / Headlines-Craniofacial Support Please contact Group Administrator / /

URL

www.headlines.org.uk / /

SocialTag