Publications by authors named "Said Trhanint"

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Investigation of 22q11.2 Deletion Syndrome in the first Moroccan Pediatric Patients series.
Asmaa Gaadi, Ahmed Aziz Bousfiha, Said Trhanint, Laila Bouguenouch, Mouna Lehlimi

Tunis Med· February 2025

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Exploring Splice-Site Mutations in LAMA2-Related Muscular Dystrophies: A Comprehensive Analysis of Genotypic and Phenotypic Patterns.
Samira Nmer, Amina Ameli, Said Trhanint, Sana Chaouki, Laila Bouguenouch

Cureus· June 2024

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Autosomal Dominant Intellectual Development Disorder-6 (MRD6) Without Seizures Linked to a De Novo Mutation in the grin2b Gene Revealed by Exome Sequencing: A Case Report of a Moroccan Child.
Hinde El Mouhi, Meriame Abbassi, Hanane Sayel, Said Trhanint, Abdelhafid Natiq

Cureus· October 2023

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Molecular and clinical assessment of maturity-onset diabetes of the young revealed low mutational rate in Moroccan families.
Said Trhanint, Laila Bouguenouch, Sana Abourazzak, Hanan El Ouahabi, Hanane Latrech

Int J Pediatr Adolesc Med· June 2022

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[Fanconi anemia at the University Hospital (CHU) Hassan II of Fez: about 6 cases].
Laila Bouguenouch, Imane Samri, Meryem Abbassi, Hasna Hamdaoui, Ihssane El Otmani, Said Trhanint

Pan Afr Med J· July 2018

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