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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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Prototypic CdLS patient from the classic (A), mild (B), and possible... | Download Scientific Diagram
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Facial phenotype of individuals with Cornelia de Lange Syndrome. a |... | Download Scientific Diagram
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Diagnosis and management of Cornelia de Lange syndrome: first international consensus statement. - Abstract - Europe PMC
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