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Prototypic CdLS patient from the classic (A), mild (B), and possible... | Download Scientific Diagram
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A Mother's Point of View - United Cerebral Palsy of Greater Cleveland
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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Genes | Free Full-Text | Cornelia de Lange Syndrome: From a Disease to a Broader Spectrum
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When Lauren turned 18, I cried for about five hours' – The Irish Times
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Cornelia de Lange syndrome
Medical Home Portal - Cornelia de Lange Syndrome
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Facial phenotype of individuals with Cornelia de Lange Syndrome. a |... | Download Scientific Diagram
Adolescents and adults affected by Cornelia de Lange syndrome: A report of 73 Italian patients - Mariani - 2016 - American Journal of Medical Genetics Part C: Seminars in Medical Genetics - Wiley Online Library
Cornelia de Lange syndrome in an adult male | Semantic Scholar
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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