11 results on '"Abbassi, Meriame"'
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2. Identification of Novel and De Novo Mutation in the SCN1A Gene By Exome Sequencing Confirms Dravet Syndrome in Moroccan Child: A Case Report
3. Autosomal Dominant Intellectual Development Disorder-6 (MRD6) Without Seizures Linked to a De Novo Mutation in the grin2b Gene Revealed by Exome Sequencing: A Case Report of a Moroccan Child
4. FLT3 Mutations in Acute Myeloid Leukemia: Unraveling the Molecular Mechanisms and Implications for Targeted Therapies
5. A homozygous missense variant in the PLCB4 gene causes severe phenotype of auriculocondylar syndrome type 2
6. A Case of Severe Teratozoospermia and Infertility Due to Homozygous Mutation c.144delC in the AURKC Gene
7. Clinical and molecular characterization of Xeroderma pigmentosum in Moroccan population: a case series of 40 patients
8. Impact of Deletion on Angelman Syndrome Phenotype Variability: Phenotype–Genotype Correlation in 97 Patients with Motor Developmental Delay
9. Syndrome de Lynch: à propos d’un cas et revue de la litterature
10. A Novel Unstable Mutation in Mitochondrial DNA Responsible for Maternally Inherited Diabetes and Deafness
11. Haplotype frequencies for 17 Y-STR loci (AmpFlSTR®Y-filer™) in a Moroccan population sample
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