![Two novel RAD21 mutations in patients with mild Cornelia de Lange syndrome-like presentation and report of the first familial case - ScienceDirect Two novel RAD21 mutations in patients with mild Cornelia de Lange syndrome-like presentation and report of the first familial case - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0378111913017228-gr1.jpg)
Two novel RAD21 mutations in patients with mild Cornelia de Lange syndrome-like presentation and report of the first familial case - ScienceDirect
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
![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
![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
![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)
Chromatinopathies: A focus on Cornelia de Lange syndrome - Avagliano - 2020 - Clinical Genetics - 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 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
![Cutaneous Manifestations of Cornelia de Lange Syndrome Clinical Presentation: History, Physical Examination Cutaneous Manifestations of Cornelia de Lange Syndrome Clinical Presentation: History, Physical Examination](https://img.medscapestatic.com/pi/meds/ckb/37/62137tn.jpg)