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PDF] Cornelia de Lange Syndrome with NIPBL Gene Mutation: A Case Report | 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
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Natural history of aging in Cornelia de Lange syndrome - Kline - 2007 - American Journal of Medical Genetics Part C: Seminars in Medical Genetics - Wiley Online Library
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