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Medicina | Free Full-Text | De novo NIPBL Mutations in Vietnamese Patients with Cornelia de Lange Syndrome
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Facial and Other Dysmorphisms of 3 Chinese Cornelia de Lange Syndrome... | Download Scientific Diagram
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
![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
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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
![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)