Frontiers | Case Report: Novel NIPBL Variants Cause Cornelia de Lange Syndrome in Chinese Patients
Stream episode Episode 53: Lauricia- Cornelia De Lange Syndrome by Orange Socks podcast | Listen online for free on SoundCloud
Cornelia de Lange Syndrome: A Variable Disorder of Cohesin Pathology | SpringerLink
Cornelia De Lange Syndrome: Practice Essentials, Pathophysiology, Epidemiology
Center for Cornelia de Lange Syndrome and Related Diagnoses | Children's Hospital of Philadelphia
A 16-Day-Old Infant with a Clinical Diagnosis of Classical Cornelia de Lange Syndrome
Cornelia de Lange Syndrome: What Is It, Causes, Signs, Symptoms, and More | Osmosis
Causes of death and autopsy findings in a large study cohort of individuals with Cornelia de Lange syndrome and review of the literature. - Abstract - Europe PMC
Fall 2012 - CdLS
Cornelia de Lange syndrome: MedlinePlus Genetics
Cornelia de Lange Syndrome: A Newborn with Imperforate Anus and a NIPBL Mutation
A novel RAD21 mutation in a boy with mild Cornelia de Lange presentation: Further delineation of the phenotype - ScienceDirect
Syndrome Cornelia de Lange - Tout Aide
Cornelia De Lange Syndrome: Practice Essentials, Pathophysiology, Epidemiology
Cornelia de Lange syndrome: MedlinePlus Genetics
Isolated NIBPL missense mutations that cause Cornelia de Lange syndrome alter MAU2 interaction | European Journal of Human Genetics
What Is Cornelia de Lange Syndrome?
Cardinal facial features of Cornelia de Lange syndrome. Facial... | Download Scientific Diagram
Genes | Free Full-Text | Cornelia de Lange Syndrome: From a Disease to a Broader Spectrum
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
Cornelia de Lange Syndrome | Children's Hospital of Philadelphia
Cornelia de Lange syndrome - Public_munhcenter
Medicina | Free Full-Text | De novo NIPBL Mutations in Vietnamese Patients with Cornelia de Lange Syndrome
