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
Comprehensive mutational analysis of a cohort of Swedish Cornelia de Lange syndrome patients | European Journal of Human Genetics
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
Cornelia de Lange syndrome: MedlinePlus Genetics
Hannah's journey with Cornelia de Lange Syndrome - Rare Disease Day 2023
A novel RAD21 mutation in a boy with mild Cornelia de Lange presentation: Further delineation of the phenotype - ScienceDirect
What are the Physical Characteristics of Cornelia de Lange Syndrome - CdLS Foundation UK and Ireland
What is Cornelia de Lange Syndrome - CdLS Foundation UK and Ireland
Medicina | Free Full-Text | De novo NIPBL Mutations in Vietnamese Patients with Cornelia de Lange Syndrome
Hannah — Same but Different
Cornelia de Lange syndrome physical characteristics
Cornelia de Lange syndrome: Year of the Zebra: Video | Osmosis
Cornelia de Lange Syndrome: What Is It, Causes, Signs, Symptoms, and More | Osmosis
Cornelia de Lange Syndrome - ScienceDirect
Frontiers | Case Report: Novel NIPBL Variants Cause Cornelia de Lange Syndrome in Chinese Patients
Cornelia de Lange Syndrome | Henry, now a happy little 15-mo… | Flickr
Isolated NIBPL missense mutations that cause Cornelia de Lange syndrome alter MAU2 interaction | European Journal of Human Genetics
The characteristic craniofacial features of Cornelia de Lange syndrome. | Download Scientific Diagram
Cornelia De Lange Syndrome: Practice Essentials, Pathophysiology, Epidemiology
