Publications by authors named "H Mossafa"

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Detection of a new deleterious gene variant in Moroccan family with inherited myoclonus-dystonia.
Faiza Chbel, Hicham Charroute, Redouane Boulouiz, Hasna Hamdaoui, Houssein Mossafa

Clin Case Rep· March 2022

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Cytogenetic and FISH analysis of 93 multiple myeloma Moroccan patients.
Hasna Hamdaoui, Oumaima Benlarroubia, Oum Kaltoum Ait Boujmia, Hossein Mossafa, Karim Ouldim

Mol Genet Genomic Med· September 2020

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Cytogenetic Resources and Information.
Etienne De Braekeleer, Jean-Loup Huret, Hossain Mossafa, Philippe Dessen

Methods Mol Biol· January 2018

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Persistent polyclonal binucleated B-cell lymphocytosis and MECOM gene amplification.
Edouard Cornet, Hossein Mossafa, Karine Courel, Jean-François Lesesve, Xavier Troussard

BMC Res Notes· March 2016

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SET-NUP214 is a recurrent γδ lineage-specific fusion transcript associated with corticosteroid/chemotherapy resistance in adult T-ALL.
Raouf Ben Abdelali, Anne Roggy, Thibaut Leguay, Agata Cieslak, Aline Renneville, Hossein Mossafa

Blood· March 2014

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