Greig cephalopolysyndactyly contiguous gene syndrome in a Congolese patient co-occurring with sickle cell anemia, and review of literature
sponsorship: No Statement Available (VLIRUOShttp://dx.doi.org/10.13039/501100022083, National Institute for Mental Health (NIMH) of the National Institutes of Health (NIH)|R01HG012284, National Institute for Mental Health (NIMH) of the National Institutes of Health (NIH)|U01MH115483, Region of Wallonia|RWAL1710180, Flemish research council (VLIR))
Authors
- Corinne Fasquelle
- Jean‐Stéphane Gatot
- Vincent Bours
- Prince Makay (ORCID: https://orcid.org/0000-0002-2910-9590)
- Aimé Lumaka (ORCID: https://orcid.org/0000-0002-5468-8678)
- Prosper Lukusa-Tshilobo (ORCID: https://orcid.org/0000-0002-5414-2915)
- Gerrye Mubungu (ORCID: https://orcid.org/0000-0002-8870-0575)
- Patrick Fuanani
- Benoît Charloteaux (ORCID: https://orcid.org/0000-0003-4282-9688)
- Léonor Palmeira (ORCID: https://orcid.org/0009-0004-8750-6692)
- Koenraad Devriendt (ORCID: https://orcid.org/0000-0002-3651-2548)
- Aimée Mupuala
- Esther Ekolo
- Ines Sonet
Institutions
- University of Kinshasa (CD)
- Center for Human Genetics (US)
- Centre Hospitalier Universitaire de Liège (BE)
- KU Leuven (BE)
Publication Details
- Journal
- Clinical Dysmorphology
- Published
- 2024-12-10
- DOI
- https://doi.org/10.1097/mcd.0000000000000510
- Primary Topic
- Hedgehog Signaling Pathway Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Vlaamse Interuniversitaire Raad
- National Institutes of Health
- National Institute of Mental Health