1p36 deletion syndrome: first case report in Morocco detected by fluorescence in situ hybridization

por Dafir, Kenza, Bouzid, Fatima Zahra, Mansouri, Maria, Aboussair, Nisrine
Publicado 2020

Spinocerebellar ataxia Type 7: clinical and genetic study of a new Moroccan family (case report)

por Bouzid, Fatima Zahra, Mansouri, Maria, Abdelaziz, Chaikhy, Louhab, Nisrine, Bernard, Sablonniere, Strubi-Vuillaume, Isabelle, Dafir, Kenza, Aboussair, Nisrine
Publicado 2021

Clinical, biochemical and molecular characterization of Wilson's disease in Moroccan patients

por Lafhal, Karima, Sabir, Es-said, Hakmaoui, Abdelmalek, Hammoud, Miloud, Aimrane, Abdelmohcine, Najeh, Samira, Assiri, Imane, Berrachid, Abdelaati, Imad, Najwa, Boujemaa, Chaima Ait, Aziz, Faissal, El Hanafi, Fatima Zahra, Lalaoui, Abdessamad, Aamri, Hasna, Boyko, Iryna, Sánchez-Monteagudo, Ana, Espinós, Carmen, Sab, Imane Ait, Aboussair, Nisrine, Bourrahouat, Aicha, Fdil, Naima
Publicado 2023

Union Makes Strength: A Worldwide Collaborative Genetic and Clinical Study to Provide a Comprehensive Survey of RD3 Mutations and Delineate the Associated Phenotype

por Perrault, Isabelle, Estrada-Cuzcano, Alejandro, Lopez, Irma, Kohl, Susanne, Li, Shiqiang, Testa, Francesco, Zekveld-Vroon, Renate, Wang, Xia, Pomares, Esther, Andorf, Jean, Aboussair, Nisrine, Banfi, Sandro, Delphin, Nathalie, den Hollander, Anneke I., Edelson, Catherine, Florijn, Ralph, Jean-Pierre, Marc, Leowski, Corinne, Megarbane, Andre, Villanueva, Cristina, Flores, Blanca, Munnich, Arnold, Ren, Huanan, Zobor, Ditta, Bergen, Arthur, Chen, Rui, Cremers, Frans P. M., Gonzalez-Duarte, Roser, Koenekoop, Robert K., Simonelli, Francesca, Stone, Edwin, Wissinger, Bernd, Zhang, Qingjiong, Kaplan, Josseline, Rozet, Jean-Michel
Publicado 2013