Amale Bousfiha

Update of the spectrum of GJB2 gene mutations in 152 Moroccan families with autosomal recessive nonsyndromic hearing loss

Amina Bakhchane, Amale Bousfiha, Hicham Charoute et al. · European Journal of Medical Genetics · 2016 · 28 citations

Developmental Biology, Mendelian Disorder, Genetic Disorder +11

Homozygous mutations in PJVK and MYO15A genes associated with non-syndromic hearing loss in Moroccan families

Sara Salime, Majida Charif, Amale Bousfiha et al. · International Journal of Pediatric Otorhinolaryngology · 2017 · 21 citations

Homozygous Mutations, Myo15a Genes, Genetic Disorder +10

Cytogenetic survey of 53 Moroccan patients with acute myeloblastic leukemia

N. Hda, B. Chadli, Amale Bousfiha et al. · Cancer Genetics and Cytogenetics · 1996 · 18 citations

Hematological Malignancy, Medicine, Moroccan Patients +8

Chronic myeloid leukemia: cytogenetics and molecular biology’s part in the comprehension and management of the pathology and treatment evolution

Sara Benchikh, Amale Bousfiha, Adil El Hamouchi et al. · Egyptian Journal of Medical Human Genetics · 2022 · 18 citations · Full text

Treatment Evolution, Kinase Inhibitors, Pathology +18

Novel compound heterozygous mutations in the GPR98 (USH2C) gene identified by whole exome sequencing in a Moroccan deaf family

Amale Bousfiha, Amina Bakhchane, Hicham Charoute et al. · Molecular Biology Reports · 2017 · 12 citations

Mendelian Disorder, Moroccan Deaf Family, Genetic Disorder +7