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Patient with an EYA1 mutation with features of branchio-oto-renal and oto-facio-cervical syndrome.

作者信息

Mercer Catherine, Gilbert Rodney, Loughlin Sam, Foulds Nicola

机构信息

Dr Catherine Mercer, Wessex Clinical Genetics Service, G Level, Mailpoint 105, Princess Anne Hospital, Coxford Road, Southampton, SO16 5YA.

出版信息

Clin Dysmorphol. 2006 Oct;15(4):211-212. doi: 10.1097/01.mcd.0000204986.54366.7c.

DOI:10.1097/01.mcd.0000204986.54366.7c
PMID:16957474
Abstract
摘要

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