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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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What are the Physical Characteristics of Cornelia de Lange Syndrome - CdLS Foundation UK and Ireland
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Cornelia de Lange Syndrome: A Case Report of a Brazilian Boy - Ana C. Scarpelli, Isabela A. Pordeus, Vera L. Resende, Lia S. Castilho, Leandro S. Marques, Saul M. Paiva, 2011
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Causes of death and autopsy findings in a large study cohort of individuals with Cornelia de Lange syndrome and review of the literature. - Abstract - Europe PMC
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Facial and Other Dysmorphisms of 3 Chinese Cornelia de Lange Syndrome... | Download Scientific Diagram
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Prenatal/neonatal pathology in two cases of Cornelia de Lange syndrome harboring novel mutations of NIPBL | Genetics in Medicine
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