Viewing StudyNCT06475651



Ignite Creation Date: 2024-07-17 @ 11:52 AM
Last Modification Date: 2024-10-26 @ 3:33 PM
Study NCT ID: NCT06475651
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-06-26
First Post: 2024-06-20

Brief Title: Characterization and Contribution of Genome-wide DNA Methylation DNA Methylation Episignatures in Rare Diseases With Prenatal Onset
Sponsor: Assistance Publique - Hôpitaux de Paris
Organization: Assistance Publique - Hôpitaux de Paris

Conditions & Keywords Data

Conditions:
Name
Rare Fetal Genetic Diseases
Congenital Malformation
Keywords:
Name View
Congenital malformation View
DNA methylation abnormalities View
Episignature View
CHD7 gene View
KMT2D gene View
HYLS1 gene View
TCTN3 gene View
FLVCR2 gene View
CHARGE syndrome View
KABUKI syndrome View