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
El Mouhi, Hinde, Abbassi, Meriame, Sayel, Hanane, Trhanint, Said, Natiq, Abdelhafid, El Hejjioui, Brahim, Jalte, Merym, Ahmadi, Youssef, Chaouki, Sana
Published in Curēus (Palo Alto, CA) (04.10.2023)
Published in Curēus (Palo Alto, CA) (04.10.2023)
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Journal Article
Clinical and molecular characterization of Xeroderma pigmentosum in Moroccan population: a case series of 40 patients
Abbassi, Meriame, Sayel, Hanane, Senhaji, Nadia, Trhanint, Said, Bay Bay, Hanane, Bouguenouch, Laila, Mernisi, Fatima Zahra
Published in Egyptian Journal of Medical Human Genetics (21.11.2022)
Published in Egyptian Journal of Medical Human Genetics (21.11.2022)
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Journal Article
Anémie de fanconi au CHU Hassan II Fès: à propos de 6 observations
Bouguenouch, Laila, Samri, Imane, Abbassi, Meryem, Hamdaoui, Hasna, Otmani, Ihssane El, Sayel, Hanane, Trhanint, Said, Benmiloud, Sara, Amrani, Moncif, Bennis, Sanae, Ouldim, Karim, Hida, Mustapha
Published in The Pan African medical journal (04.12.2017)
Published in The Pan African medical journal (04.12.2017)
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Journal Article
Exploring Splice-Site Mutations in LAMA2-Related Muscular Dystrophies: A Comprehensive Analysis of Genotypic and Phenotypic Patterns
Nmer, Samira, Ameli, Amina, Trhanint, Said, Chaouki, Sana, Bouguenouch, Laila, Ouldim, Karim
Published in Curēus (Palo Alto, CA) (03.06.2024)
Published in Curēus (Palo Alto, CA) (03.06.2024)
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Journal Article
Molecular and clinical assessment of maturity-onset diabetes of the young revealed low mutational rate in Moroccan families
Trhanint, Said, Bouguenouch, Laila, Abourazzak, Sana, El Ouahabi, Hanan, Latrech, Hanane, Benyakhlef, Salma, Bennani, Bahia, El Bouchikhi, Ihssane, Moufid, Fatima Zahra, Ouldim, Karim, El Ghadraoui, Lahsen, Maazouzi, Nadia
Published in International journal of pediatrics & adolescent medicine (01.06.2022)
Published in International journal of pediatrics & adolescent medicine (01.06.2022)
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Journal Article
Anémie de fanconi au CHU Hassan II Fès: à propos de 6 observations
Bouguenouch, Laila, Samri, Imane, Abbassi, Meryem, Hamdaoui, Hasna, El Otmani, Ihssane, Sayel, Hanane, Trhanint, Said, Benmiloud, Sara, Amrani, Moncif, Bennis, Sanae, Ouldim, Karim, Hida, Mustapha
Published in The Pan African medical journal (2017)
Published in The Pan African medical journal (2017)
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Journal Article
Fanconi anemia at the University Hospital (CHU) Hassan II of Fez: about 6 cases
Bouguenouch, Laila, Samri, Imane, Abbassi, Meryem, Hamdaoui, Hasna, Otmani, Ihssane El, Sayel, Hanane, Trhanint, Said, Benmiloud, Sara, Amrani, Moncif, Bennis, Sanae, Ouldim, Karim, Hida, Mustapha
Published in The Pan African medical journal (2017)
Published in The Pan African medical journal (2017)
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Journal Article
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
El Mouhi, Hinde, Abbassi, Meriame, Sayel, Hanane, Trhanint, Said, Natiq, Abdelhafid, El Hejjioui, Brahim, Jalte, Merym, Ahmadi, Youssef, Chaouki, Sana
Published in Cureus (01.10.2023)
Published in Cureus (01.10.2023)
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