![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
![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
![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)
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 RAD21 mutation in a boy with mild Cornelia de Lange presentation: Further delineation of the phenotype - ScienceDirect A novel RAD21 mutation in a boy with mild Cornelia de Lange presentation: Further delineation of the phenotype - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S176972121830363X-gr1.jpg)
A novel RAD21 mutation in a boy with mild Cornelia de Lange presentation: Further delineation of the phenotype - ScienceDirect
![Genotype-phenotype correlations of 39 patients with Cornelia De Lange syndrome: the Dutch experience | Journal of Medical Genetics Genotype-phenotype correlations of 39 patients with Cornelia De Lange syndrome: the Dutch experience | Journal of Medical Genetics](https://jmg.bmj.com/content/jmedgenet/43/7/568/F2.large.jpg)
Genotype-phenotype correlations of 39 patients with Cornelia De Lange syndrome: the Dutch experience | Journal of Medical Genetics
![Causes of death and autopsy findings in a large study cohort of individuals with Cornelia de Lange syndrome and review of the literature - Schrier - 2011 - American Journal of Medical Causes of death and autopsy findings in a large study cohort of individuals with Cornelia de Lange syndrome and review of the literature - Schrier - 2011 - American Journal of Medical](https://onlinelibrary.wiley.com/cms/asset/72a11ba4-cfdf-49b5-bf0e-c7f7edd4eedd/mfig001.jpg)
Causes of death and autopsy findings in a large study cohort of individuals with Cornelia de Lange syndrome and review of the literature - Schrier - 2011 - American Journal of Medical
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)