8 results on '"Laarabi, Fatima Zahra"'
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2. Identification of a novel LAMA2 c.2217G > A, p.(Trp739*) mutation in a Moroccan patient with congenital muscular dystrophy: a case report
3. Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly
4. A novel single variant in the MEFV gene causing Mediterranean fever and Behçet’s disease: a case report
5. A novel frameshift mutation in the XPC gene in a Moroccan patient: a case report
6. 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
7. Further evidence for causal FAM20A mutations and first case of amelogenesis imperfecta and gingival hyperplasia syndrome in Morocco: a case report
8. Distribution of allelic and genotypic frequencies of NAT2 and CYP2E1variants in Moroccan population
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