Hind Dehbi

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

Association of glutathione S-transferase (GSTM1 and GSTT1) genes with chronic myeloid leukemia

Yaya Kassogué, Hind Dehbi, Meryem Quachouh et al. · SpringerPlus · 2015 · 23 citations · Full text

Functional polymorphism of CYP2B6 G15631T is associated with hematologic and cytogenetic response in chronic myeloid leukemia patients treated with imatinib

Yaya Kassogué, Meryem Quachouh, Hind Dehbi et al. · Medical Oncology · 2013 · 20 citations

Cyp2b6 G15631t, Chromatin, Hematological Malignancy +10

Genotype Variability and Haplotype Frequency of <i>MDR1</i> ( <i>ABCB1</i> ) Gene Polymorphism in Morocco

Yaya Kassogué, Hind Dehbi, Sanaa Nassereddine et al. · DNA and Cell Biology · 2013 · 20 citations

Single nucleotide polymorphisms of multidrug resistance gene 1 (MDR1) and risk of chronic myeloid leukemia

Yaya Kassogué, Hind Dehbi, Quachouh Meryem et al. · Tumor Biology · 2014 · 18 citations