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 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](https://onlinelibrary.wiley.com/cms/asset/be233542-5b59-43db-b131-fbeac927660a/ccr31010-fig-0001-m.jpg)
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
Ezra is diagnosed with Cornelia de Lange syndrome, which causes a mutation in certain genes. Upon learning of his heart defects… | Instagram
![Facial and Other Dysmorphisms of 3 Chinese Cornelia de Lange Syndrome... | Download Scientific Diagram Facial and Other Dysmorphisms of 3 Chinese Cornelia de Lange Syndrome... | Download Scientific Diagram](https://www.researchgate.net/publication/323226784/figure/fig1/AS:614165722955779@1523439927048/Facial-and-Other-Dysmorphisms-of-3-Chinese-Cornelia-de-Lange-Syndrome-Neonates-All-three.png)
Facial and Other Dysmorphisms of 3 Chinese Cornelia de Lange Syndrome... | Download Scientific Diagram
![Cornelia de Lange Syndrome: A Case Report with a Novel Congenital Heart Disease Association | Journal of Comprehensive Pediatrics | Full Text Cornelia de Lange Syndrome: A Case Report with a Novel Congenital Heart Disease Association | Journal of Comprehensive Pediatrics | Full Text](https://services.brieflands.com/cdn/serve/315e3/9c118f2773631bed66b4f5e3481a4be5c6b81f0c/jcp-13-4-129997-g001-preview.png)
Cornelia de Lange Syndrome: A Case Report with a Novel Congenital Heart Disease Association | Journal of Comprehensive Pediatrics | Full Text
![Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B | Nature Genetics Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B | Nature Genetics](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fng1364/MediaObjects/41588_2004_Article_BFng1364_Fig1_HTML.jpg)
Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B | Nature Genetics
![Cornelia de Lange syndrome: To diagnose or not to diagnose in utero? - Avagliano - 2017 - Birth Defects Research - Wiley Online Library Cornelia de Lange syndrome: To diagnose or not to diagnose in utero? - Avagliano - 2017 - Birth Defects Research - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/441db85c-b0f4-44a5-81ec-99bf0c2abd28/bdr21045-fig-0001-m.jpg)
Cornelia de Lange syndrome: To diagnose or not to diagnose in utero? - Avagliano - 2017 - Birth Defects Research - Wiley Online Library
![Syndrome Cornelia de Lange : quelles sont les causes de cette maladie dont est décédée une petite fille ? Syndrome Cornelia de Lange : quelles sont les causes de cette maladie dont est décédée une petite fille ?](https://www.pourquoidocteur.fr/media/article/istock-698165894-1642688910.jpg)
Syndrome Cornelia de Lange : quelles sont les causes de cette maladie dont est décédée une petite fille ?
![The characteristic craniofacial features of Cornelia de Lange syndrome. | Download Scientific Diagram The characteristic craniofacial features of Cornelia de Lange syndrome. | Download Scientific Diagram](https://www.researchgate.net/publication/234100200/figure/fig5/AS:324129615040526@1454289930690/The-characteristic-craniofacial-features-of-Cornelia-de-Lange-syndrome.png)
The characteristic craniofacial features of Cornelia de Lange syndrome. | Download Scientific Diagram
![Medicina | Free Full-Text | De novo NIPBL Mutations in Vietnamese Patients with Cornelia de Lange Syndrome Medicina | Free Full-Text | De novo NIPBL Mutations in Vietnamese Patients with Cornelia de Lange Syndrome](https://www.mdpi.com/medicina/medicina-56-00076/article_deploy/html/images/medicina-56-00076-g001.png)
Medicina | Free Full-Text | De novo NIPBL Mutations in Vietnamese Patients with Cornelia de Lange Syndrome
![Chromatinopathies: A focus on Cornelia de Lange syndrome - Avagliano - 2020 - Clinical Genetics - Wiley Online Library Chromatinopathies: A focus on Cornelia de Lange syndrome - Avagliano - 2020 - Clinical Genetics - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/37590899-b17c-4395-816d-e8307cfcd73f/cge13674-fig-0001-m.jpg)