Fatima Zahra Laarabi

Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly

Najim Lahrouchi, Aman George, Ilham Ratbi et al. · Nature Communications · 2019 · 38 citations · Full text

Distribution of allelic and genotypic frequencies of NAT2 and CYP2E1variants in Moroccan population

Soukaina Guaoua, Ilham Ratbi, Fatima Zahra Laarabi et al. · BMC Genetics · 2014 · 37 citations · Full text

Genetic testing and first presymptomatic diagnosis in Moroccan families at high risk for breast/ovarian cancer

Fatima Zahra Laarabi, Imane Cherkaoui Jaouad, Karim Ouldim et al. · Oncology Letters · 2011 · 26 citations · Full text

Brca2 Genes, Dna Genetic Testing, Genetic Testing +14

Carrier Frequency of the c.525delT Mutation in the <i>SGCG</i> Gene and Estimated Prevalence of Limb Girdle Muscular Dystrophy Type 2C Among the Moroccan Population

F. El Kerch, Ilham Ratbi, Aziza Sbiti et al. · Genetic Testing and Molecular Biomarkers · 2014 · 24 citations

High frequency of the recurrent c.1310_1313delAAGA BRCA2 mutation in the North-East of Morocco and implication for hereditary breast–ovarian cancer prevention and control

Fatima Zahra Laarabi, Ilham Ratbi, Siham Chafai Elalaoui et al. · BMC Research Notes · 2017 · 23 citations · Full text