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The characteristic craniofacial features of Cornelia de Lange syndrome. | Download Scientific Diagram
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Medicina | Free Full-Text | De novo NIPBL Mutations in Vietnamese Patients with Cornelia de Lange Syndrome
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Cornelia de Lange syndrome: To diagnose or not to diagnose in utero? - Avagliano - 2017 - Birth Defects Research - Wiley Online Library
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Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B | Nature Genetics
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Further Characterization of SMC1A Loss of Function Epilepsy Distinct From Cornelia de Lange Syndrome - Kristin W. Barañano, Amy Kimball, Susan L. Fong, Alena S. Egense, Catherine Hudon, Antonie D. Kline, 2022
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Chromatinopathies: A focus on Cornelia de Lange syndrome - Avagliano - 2020 - Clinical Genetics - Wiley Online Library
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Cornelia de Lange Syndrome: A Case Report with a Novel Congenital Heart Disease Association | Journal of Comprehensive Pediatrics | Full Text
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PSODCareForRare on X: "What is CDLS or Cornelia de Lange Syndrome? What are the signs? Visit the @CdLSFoundation instagram acct for their interactive post. Honoring the people living with #CDLS on this
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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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