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Hasna Hamdaoui

Human genome meeting 2016
2016 · GUSTO study group, A. K. Srivastava, et al. · Human Genomics · 41
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Cytogenetic and FISH analysis of 93 multiple myeloma Moroccan patients
2020 · Hasna Hamdaoui, Oumaima Benlarroubia, et al. · Molecular Genetics & Genomic Medicine · 16
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Multiple Myeloma: Bioinformatic Analysis for Identification of Key Genes and Pathways
2022 · Chaimaa Saadoune, Badreddine Nouadi, et al. · Bioinformatics and Biology Insights · 13
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Report of a New Case of Pentasomy X Revealed by Status Epilepticus
2021 · Nabila Chekhlabi, Amal Haoudar, et al. · Cureus · 4
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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
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Misdiagnosis of Tracher-Collins Syndrome Initially Attributed to Drug Teratogenicity: A Moroccan Case Report
2023 · A Lamzouri, A EL Rherbi, et al. · Balkan Journal of Medical Genetics · 2
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Near tetrapoloid karyotype with translocation t(11;14) in a Moroccan patient with amyloid light-chain amyloidosis and multiple myeloma
2020 · Hasna Hamdaoui, Abdelhafid Natiq, et al. · Leukemia Research Reports · 2
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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
[Microdeletion syndromes (Williams syndrome and deletion syndrome 22q11) at CHU Hassan II of Fez: report of 3 observations].
2012 · Karim Ouldim, Laila Bouguenouch, et al. · PubMed · 1
Cytogenetic abnormalities correlate with clinico-biological characteristics in 30 Moroccan multiple myeloma patients
2023 · Hasna Hamdaoui, Badreddine Nouadi, et al. · Leukemia Research Reports
Rare chromosomal translocations associated with pediatric case of AML cup like: t(4;12)(q12; p13), t(1;16)(q12;q24) and t(12;13)(p13;q13)
2022 · Hamdaoui Hasna, Abdelhafid Natiq, et al.
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Detection of a new deleterious SGCE gene variant in Moroccan family with inherited Myoclonic-dystonia
2021 · chbel faiza, charoute hicham, et al.
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Analysis of protein overexpression and Her2 gene amplification in gastric adenocarcinoma from Moroccan patients
2018 · L. Fahmi, H. Fettachi, et al. · European Journal of Cancer
Anémie de fanconi au CHU Hassan II Fès: à propos de 6 observations
2017 · Laila Bouguenouch, Imane Samri, et al. · Pan African Medical Journal
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Marqueurs chromosomiques: à propos d'un cas
2013 · Imane Samri, Laila Bouguenouch, et al. · Pan African Medical Journal
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[The Cri du Chat syndrome: report of an observation].
2012 · Karim Ouldim, Imane Samri, et al. · PubMed
Works count: 16
Citation count: 82
H-index: 4
I10-index: 3
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