DLL1 haploinsufficiency in prenatal brain anomalies: a retrospective analysis of 6q terminal deletions
Objective6q terminal deletion is a rare genetic cause of prenatal brain anomalies. We evaluated five cases of cerebral dysplasia within a familial context for genetic diagnosis. Aims to analyze prenatal brain abnormalities from 6q terminal deletion of DLL1 and support prenatal diagnosis and genetic...
Gespeichert in:
| Hauptverfasser: | , , , , , , , , |
|---|---|
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Frontiers Media S.A.
2025-10-01
|
| Schriftenreihe: | Frontiers in Genetics |
| Schlagworte: | |
| Online-Zugang: | https://www.frontiersin.org/articles/10.3389/fgene.2025.1640775/full |
| Tags: |
Keine Tags, Fügen Sie das erste Tag hinzu!
|