Author

Houssein Mossafa

Observed names: MOSSAFA Houssein, Mossafa Houssein

Institution: Université Mohammed VI des Sciences et de la Santé

Observed institutions: Instituts Supérieurs des Professions Infirmières et Techniques de Santé, Laboratoire National de Référence, Université Mohammed VI des Sciences et de la Santé

OpenAlex ID: A5012089573

Conventional and molecular cytogenetic characterization of a Moroccan patient with WAGR syndrome

2024 · Faiza Chbel, Hasna Hamdaoui, et al. · Egyptian Journal of Medical Human Genetics · 2

Detection of a new deleterious SGCE gene variant in Moroccan family with inherited myoclonus–dystonia

2022 · Faiza Chbel, Hicham Charroute, et al. · Clinical Case Reports · 1

Assessment of STRs Loci on Investigator Id-Plex Plus Kit for Forensics and Chimerism Monitoring in Morocco: A Case Series

2023 · CHBEL Faiza, EL ARJI Marzouk, et al. · Zenodo (CERN European Organization for Nuclear Research)

Detection of a new deleterious SGCE gene variant in Moroccan family with inherited Myoclonic-dystonia

2021 · chbel faiza, charoute hicham, et al.

Works count: 4

Citation count: 3

H-index: 1

I10-index: