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Two novel RAD21 mutations in patients with mild Cornelia de Lange syndrome-like presentation and report of the first familial case. | Semantic Scholar
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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A novel RAD21 mutation in a boy with mild Cornelia de Lange presentation: Further delineation of the phenotype - ScienceDirect
Chromatinopathies: A focus on Cornelia de Lange syndrome - Avagliano - 2020 - Clinical Genetics - Wiley Online Library
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Facial phenotype of individuals with Cornelia de Lange Syndrome. a |... | Download Scientific Diagram
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The characteristic craniofacial features of Cornelia de Lange syndrome. | Download Scientific Diagram
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CENTOGENE - Did you know? #DUK Cornelia de Lange #Didyouknow Cornelia de Lange syndrome (CdLS) is a syndromic disorder, with symptoms that include distinctive facial features including arched eyebrows that often meet
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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![PDF] Cornelia de Lange Syndrome with NIPBL Gene Mutation: A Case Report | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/abaf947324ff8da41163636eda8319e9ac599c41/2-Figure1-1.png "PDF] Cornelia de Lange Syndrome with NIPBL Gene Mutation: A Case Report | Semantic Scholar")