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Two novel RAD21 mutations in patients with mild Cornelia de Lange syndrome-like presentation and report of the first familial case - ScienceDirect
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Medicina | Free Full-Text | De novo NIPBL Mutations in Vietnamese Patients with Cornelia de Lange Syndrome
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Facial and Other Dysmorphisms of 3 Chinese Cornelia de Lange Syndrome... | Download Scientific Diagram
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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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
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The characteristic craniofacial features of Cornelia de Lange syndrome. | Download Scientific Diagram
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Isolated NIBPL missense mutations that cause Cornelia de Lange syndrome alter MAU2 interaction | European Journal of Human Genetics
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Chromatinopathies: A focus on Cornelia de Lange syndrome - Avagliano - 2020 - Clinical Genetics - Wiley Online Library
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About the Center for Cornelia de Lange Syndrome and Related Diagnoses | Children's Hospital of Philadelphia
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