Cornelia De Lange Syndrome Karyotype Collection Mode [2022] Cornelia De Lange Syndrome Karyotype Collection Mode [2022]

Cornelia De Lange Syndrome Karyotype

Dec. 25, 2024

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


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