12 results on '"Taher, Mohamed B."'
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2. Expanding the phenotypic spectrum and clinical severity associated with WLS gene
3. Studying the pathogenicity of 26 variants characterized in the first molecular analyses of Egyptian aplastic anemia patients
4. Importance of TREC and KREC as molecular markers for immunological evaluation of down syndrome children
5. Defining the molecular pathology and consequent phenotypes in Egyptian HB patients
6. Corrigendum to “Defining the molecular pathology and consequent phenotypes in Egyptian HB patients” [J. Genet. Eng. Biotechnol. 19(1) (2021) 75]
7. Outlining the Clinical Profile of TCIRG1 14 Variants including 5 Novels with Overview of ARO Phenotype and Ethnic Impact in 20 Egyptian Families
8. Genetic Implications in High-Risk Pregnancy and Its Outcome: A 2-Year Study.
9. Genetic Implications in High-Risk Pregnancy and Its Outcome: A 2-Year Study
10. Unilateral Isolated Proximal Femoral Focal Deficiency in an Egyptian Infant and Review of Literature
11. Further delineation of the oculoauricular syndrome phenotype: A new family with a novel truncating HMX1 mutation
12. Further delineation of the oculoauricular syndrome phenotype: A new family with a novel truncating HMX1 mutation.
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