![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 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](https://pbs.twimg.com/media/EXiqtPVUMAAIK75.jpg)
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
![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
![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
Madmoiz'elle Mya: son quotidien avec le syndrome cornelia de lange. - Bonsoir !! Mya passe de bonnes vacances ! Entre journée grasse mat', grosse sieste Et levé très tôt mais zéro sieste
![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
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
![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
![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
![What are the Physical Characteristics of Cornelia de Lange Syndrome - CdLS Foundation UK and Ireland What are the Physical Characteristics of Cornelia de Lange Syndrome - CdLS Foundation UK and Ireland](https://www.cdls.org.uk/media/images/CdLS%20Figure%203.png)
What are the Physical Characteristics of Cornelia de Lange Syndrome - CdLS Foundation UK and Ireland
![A novel mutation in NIPBL3 in a case of Cornelia de Lange syndrome confirmed with genetic testing following intrauterine fetal death | Journal of Clinical Pathology A novel mutation in NIPBL3 in a case of Cornelia de Lange syndrome confirmed with genetic testing following intrauterine fetal death | Journal of Clinical Pathology](https://jcp.bmj.com/content/jclinpath/67/3/283/F1.large.jpg)