![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")
PDF] Cornelia de Lange Syndrome with NIPBL Gene Mutation: A Case Report | Semantic Scholar
Mausbeere Annikas Blog / Cornelia de Lange - Syndrom / CdLS: April 2019
Genes | Free Full-Text | Cornelia de Lange Syndrome: From a Disease to a Broader Spectrum
A novel RAD21 mutation in a boy with mild Cornelia de Lange presentation: Further delineation of the phenotype - ScienceDirect
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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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