Cornelia De Lange Syndrome Karyotype
March 16, 2025
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 Frontiers | Case Report: Novel NIPBL Variants Cause Cornelia de Lange Syndrome in Chinese Patients Cornelia de Lange syndrome: MedlinePlus Genetics Cornelia De Lange Syndrome Karyotype