Mohamed B. Taher

Cairo, C, Egypt

Last Updated: 09/26/2026

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Found 13 publications

Molecular and Clinical Characterization of a Cohort of Autosomal Recessive Sensorineural Hearing Loss in Egyptian Patients.

Molecular and Clinical Characterization of a Cohort of Autosomal Recessive Sensorineural Hearing Loss in Egyptian Patients.

Journal: Journal of molecular neuroscience : MN

Published: August 20, 2024

Corrigendum to "Defining the molecular pathology and consequent phenotypes in Egyptian HB patients" [J. Genet. Eng. Biotechnol. 19(1) (2021) 75].

Corrigendum to "Defining the molecular pathology and consequent phenotypes in Egyptian HB patients" [J. Genet. Eng. Biotechnol. 19(1) (2021) 75].

Journal: Journal, genetic engineering & biotechnology

Published: May 26, 2024

Insight into Apert Syndrome: Reporting on Six Patients and Increasing Awareness.

Insight into Apert Syndrome: Reporting on Six Patients and Increasing Awareness.

Journal: Molecular neurobiology

Published: May 01, 2024

Genetic Correlation of HBB, HFE and HAMP Genes to Endocrinal Complications in Egyptian Beta Thalassemia Major Patients.

Genetic Correlation of HBB, HFE and HAMP Genes to Endocrinal Complications in Egyptian Beta Thalassemia Major Patients.

Journal: Biochemical genetics

Published: March 03, 2024

Importance of TREC and KREC as molecular markers for immunological evaluation of down syndrome children.

Importance of TREC and KREC as molecular markers for immunological evaluation of down syndrome children.

Journal: Scientific reports

Published: July 19, 2023

Studying the pathogenicity of 26 variants characterized in the first molecular analyses of Egyptian aplastic anemia patients.

Studying the pathogenicity of 26 variants characterized in the first molecular analyses of Egyptian aplastic anemia patients.

Journal: Journal, genetic engineering & biotechnology

Published: July 14, 2023

Evaluation of Sleep Difficulties in Egyptian Children with Down Syndrome: A Case-Control Study.

Evaluation of Sleep Difficulties in Egyptian Children with Down Syndrome: A Case-Control Study.

Journal: Indian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India

Published: June 23, 2023

Expanding the phenotypic spectrum and clinical severity associated with WLS gene.

Expanding the phenotypic spectrum and clinical severity associated with WLS gene.

Journal: Journal of human genetics

Published: January 21, 2023

Outlining the Clinical Profile of TCIRG1 14 Variants including 5 Novels with Overview of ARO Phenotype and Ethnic Impact in 20 Egyptian Families.

Outlining the Clinical Profile of TCIRG1 14 Variants including 5 Novels with Overview of ARO Phenotype and Ethnic Impact in 20 Egyptian Families.

Journal: Genes

Published: November 29, 2022

Oro-dental features in Egyptian patients with familial mediterranean fever.

Oro-dental features in Egyptian patients with familial mediterranean fever.

Journal: Special care in dentistry : official publication of the American Association of Hospital Dentists, the Academy of Dentistry for the Handicapped, and the American Society for Geriatric Dentistry

Published: September 09, 2021

Defining the molecular pathology and consequent phenotypes in Egyptian HB patients.

Defining the molecular pathology and consequent phenotypes in Egyptian HB patients.

Journal: Journal, genetic engineering & biotechnology

Published: January 29, 2021

Further delineation of the oculoauricular syndrome phenotype: A new family with a novel truncating HMX1 mutation.

Further delineation of the oculoauricular syndrome phenotype: A new family with a novel truncating HMX1 mutation.

Journal: Ophthalmic genetics

Published: November 16, 2017

Showing 1-12 of 13

Last Updated: 09/26/2026