First Prenatal Case of Genotypically and Phenotypically Overlapping Double Molecular Diagnosis of Van den Ende–Gupta and 22q11.2 Deletion Syndromes
Authors
- Thierry Rousseau (ORCID: https://orcid.org/0000-0002-9386-6668)
- Caroline Racine (ORCID: https://orcid.org/0000-0003-2378-5982)
- Olivia Martz
- Laurence Olivier Faivre (ORCID: https://orcid.org/0000-0001-9770-444X)
- Julien Maraval (ORCID: https://orcid.org/0009-0003-6744-5821)
- Hana Safraou (ORCID: https://orcid.org/0000-0002-1726-9474)
- Christel Thauvin‐Robinet
- Aurore Garde (ORCID: https://orcid.org/0000-0003-3196-0453)
- Fara T. Harizay
- Ange‐Line Bruel (ORCID: https://orcid.org/0000-0002-0526-465X)
- Nathalie Marle (ORCID: https://orcid.org/0000-0001-7628-3869)
- Vinciane Eluard
- L. Martin
- Christophe Philippe
Institutions
- Inserm (FR)
- Université de Bourgogne (FR)
- Hôpital d'Enfants (FR)
- CHU Dijon Bourgogne (FR)
Publication Details
- Journal
- Molecular Genetics & Genomic Medicine
- Published
- 2025-04-01
- DOI
- https://doi.org/10.1002/mgg3.70096
- Primary Topic
- Congenital heart defects research
- Type
- article
- Field-Weighted Citation Impact
- 0.00