Afaf Lamzouri
Tangier, Morocco
Last Updated: 09/26/2026
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Found 12 publications
Common cutaneous signs unmasking a severe hematological disorder: GATA2 deficiency.
Journal: Dermatology online journal
Published: December 29, 2025
Microcephaly, Epilepsy, and Diabetes Syndrome 1: A Moroccan Case Report of Novel Compound Heterozygous IER3IP1 Mutations and Literature Review.
Journal: Balkan journal of medical genetics : BJMG
Published: November 07, 2025
SeqExpressionAnalyser: An R Package for Automated End-to-End RNA-Seq Analysis From Reads to Differential Expression.
Journal: Bioinformatics and biology insights
Published: April 22, 2025
Adoption of an in-silico analysis approach to assess the functional and structural impacts of rpoB-encoded protein mutations on Chlamydia pneumoniae sensitivity to antibiotics.
Journal: BMC microbiology
Published: September 20, 2024
Hematological ABP: Interest of New Generation Sequencing Methods (NGS) to Study Suspicious Fluctuations in Erythropoiesis.
Journal: Drug testing and analysis
Published: July 08, 2024
Misdiagnosis of Tracher-Collins Syndrome Initially Attributed to Drug Teratogenicity: A Moroccan Case Report.
Journal: Balkan journal of medical genetics : BJMG
Published: March 14, 2024
Cytogenetic abnormalities correlate with clinico-biological characteristics in 30 Moroccan multiple myeloma patients.
Journal: Leukemia research reports
Published: August 28, 2023
Low prevalence of p.G352fsdelG mutation in phenylketonuria patients from Morocco.
Journal: Genetic testing and molecular biomarkers
Published: July 20, 2012
Prenatal diagnosis of trisomy 21 by fluorescence in situ hybridization (FISH): about the first tests in Morocco
Journal: The Pan African medical journal
Published: May 16, 2012
Russell Silver syndrome: report of three cases and review of the literature
Journal: The Pan African medical journal
Published: March 15, 2012
Showing 1-12 of 12
Last Updated: 09/26/2026