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About the Center for Cornelia de Lange Syndrome and Related Diagnoses | Children's Hospital of Philadelphia
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Rare form of autosomal dominant familial Cornelia de Lange syndrome due to a novel duplication in SMC3 - Infante - 2017 - Clinical Case Reports - Wiley Online Library
Hi my name is Freya and I have Cornelia de Lange Syndrome. Next Saturday is CDLS awareness day. So this week I will be sharing my journey.… | Instagram
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The characteristic craniofacial features of Cornelia de Lange syndrome. | Download Scientific Diagram
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