Hanan H. Afifi

Cairo, C, Egypt

Last Updated: 09/26/2026

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Found 35 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

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

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

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

Multiplex ligation-dependent probe amplification versus fluorescent in situ hybridization for screening RB1 copy number variations in Egyptian patients with retinoblastoma.

Multiplex ligation-dependent probe amplification versus fluorescent in situ hybridization for screening RB1 copy number variations in Egyptian patients with retinoblastoma.

Journal: Ophthalmic genetics

Published: September 13, 2022

Further Evidence of a Continuum in the Clinical Spectrum of Dominant PIEZO2-Related Disorders and Implications in Cerebellar Anomalies.

Further Evidence of a Continuum in the Clinical Spectrum of Dominant PIEZO2-Related Disorders and Implications in Cerebellar Anomalies.

Journal: Molecular syndromology

Published: January 09, 2022

Genetic Implications in High-Risk Pregnancy and Its Outcome: A 2-Year Study.

Genetic Implications in High-Risk Pregnancy and Its Outcome: A 2-Year Study.

Journal: American journal of perinatology

Published: February 26, 2021

Chromosome 9p terminal deletion in nine Egyptian patients and narrowing of the critical region for trigonocephaly.

Chromosome 9p terminal deletion in nine Egyptian patients and narrowing of the critical region for trigonocephaly.

Journal: Molecular genetics & genomic medicine

Published: January 03, 2021

Erratum: Clinical Variability of Pallister-Killian Syndrome in Two Egyptian Patients.

Erratum: Clinical Variability of Pallister-Killian Syndrome in Two Egyptian Patients.

Journal: Journal of pediatric genetics

Published: September 01, 2020

Clinical and Cytogenomic Characterization of De Novo 11p14.3-p15.5 Duplication Associated with 18q23 Deletion in an Egyptian Female Infant.

Clinical and Cytogenomic Characterization of De Novo 11p14.3-p15.5 Duplication Associated with 18q23 Deletion in an Egyptian Female Infant.

Journal: Journal of pediatric genetics

Published: November 10, 2019

Microcephalic osteodysplastic primordial dwarfism type II: Additional nine patients with implications on phenotype and genotype correlation.

Microcephalic osteodysplastic primordial dwarfism type II: Additional nine patients with implications on phenotype and genotype correlation.

Journal: American journal of medical genetics. Part A

Published: July 09, 2019

Clinical Variability of Pallister-Killian Syndrome in Two Egyptian Patients.

Clinical Variability of Pallister-Killian Syndrome in Two Egyptian Patients.

Journal: Journal of pediatric genetics

Published: June 22, 2019

Showing 1-12 of 35

Last Updated: 09/26/2026