Mar Borregán Prats
Investigador post-doc
Research group
Professional network profiles
Last Publications
- Luque-Luna M, Borregán M, Lianes JG and Prat-Torres CS Waardenburg syndrome. MEDICINA CLINICA . 164(2): 105-106.
- Charach, R, Pérez-Cruz M, Masoller-Casas N, Illa-Armengol M, Monterde, E, Martínez-Crespo, JM, Borrell, A, Gómez-Chiari M, Rebollo M, Borregán M, Gómez, O and Eixarch, E Systematic Ultrasound Evaluation of Olfactory Sulci in Fetuses with Congenital Heart Defects: A Clue for CHARGE Syndrome Diagnosis. FETAL DIAGNOSIS AND THERAPY . 52(3): 280-290.
- Hernando-Davalillo C, Alcalá-San Martin A, Borregán M and Ortigoza-Escobar JD De novo 4q35.2 duplication containing FAT1 is associated with autism spectrum disorder CLINICAL GENETICS . 102(5): 434-437.
Projects
- Project name:
- SGR 2022-2024_Precision Medicine of Genetic and Rare Diseases (PrecisionRare)
- Leader
- Francesc Palau Martínez
- Funding entities:
- Agaur - Agència de Gestió d'Ajuts Universitaris i de Recerca
- Code
- 2021 SGR 01610
- Starting - finishing date:
- 2022 - 2025
