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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 - ScienceDirect
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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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Isolated NIBPL missense mutations that cause Cornelia de Lange syndrome alter MAU2 interaction | European Journal of Human Genetics
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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
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
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Chromatinopathies: A focus on Cornelia de Lange syndrome - Avagliano - 2020 - Clinical Genetics - Wiley Online Library
![Stream episode Episode 53: Lauricia- Cornelia De Lange Syndrome by Orange Socks podcast | Listen online for free on SoundCloud Stream episode Episode 53: Lauricia- Cornelia De Lange Syndrome by Orange Socks podcast | Listen online for free on SoundCloud](https://i1.sndcdn.com/artworks-000229309569-8jylwh-t500x500.jpg)
Stream episode Episode 53: Lauricia- Cornelia De Lange Syndrome by Orange Socks podcast | Listen online for free on SoundCloud
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