Ghada M. Elhady
Alexandria, ALX, Egypt
Last Updated: 09/26/2026
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Found 10 publications
Lessons learned from the exome sequencing of nine cases of infertility and the way forward.
Journal: Reproductive biomedicine online
Published: July 28, 2025
A homozygous nonsense variant in the alternatively spliced VLDLR exon 4 causes a neurodevelopmental disorder without features of VLDLR cerebellar hypoplasia.
Journal: Journal of human genetics
Published: April 22, 2024
The Use of Fluorescence In situ Hybridisation in the Diagnosis of Hidden Mosaicism in Egyptian Patients with Turner Syndrome.
Journal: Journal of human reproductive sciences
Published: September 27, 2023
Familial reciprocal non robertsonian translocation t(14;22) resulting in 22q11.2 deletion syndrome.
Journal: The Turkish journal of pediatrics
Published: February 28, 2020
Chromosomal Aberrations in 224 Couples with Recurrent Pregnancy Loss.
Journal: Journal of human reproductive sciences
Published: February 04, 2020
The Association Between Interleukin 1 Beta Promoter Polymorphisms And Keratoconus Incidence And Severity In An Egyptian Population.
Journal: Clinical ophthalmology (Auckland, N.Z.)
Published: June 25, 2019
De novo EDA mutations: Variable expression in two Egyptian families.
Journal: Archives of oral biology
Published: December 23, 2015
Novel PITX2 gene mutations in patients with Axenfeld-Rieger syndrome.
Journal: Acta ophthalmologica
Published: June 24, 2015
Showing 1-10 of 10
Last Updated: 09/26/2026