Ebtesam M. Abdalla
Alexandria, ALX, Egypt
Last Updated: 09/26/2026
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Found 63 publications
Report of two patients with variants in FOXL2 and KASH5 and review of gestational trophoblastic neoplasia after recurrent moles.
Journal: Journal of assisted reproduction and genetics
Published: June 02, 2026
The importance of integrating genetic testing into reproductive medicine: a retrospective observational study investigating the monogenic causes of human infertility in couples considering ICSI.
Journal: Journal of human genetics
Published: March 04, 2026
RNU4ATAC-opathy: Clinical, molecular and transcriptomic insights from a large cohort.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: October 13, 2025
RNU4ATAC-opathy: Clinical, molecular, and transcriptomic insights from a large cohort.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: October 13, 2025
Growth hormone deficiency in three siblings homozygous for a rare GH1 haplotype.
Journal: Frontiers in endocrinology
Published: September 14, 2025
Exploring the molecular basis of microphthalmia and anophthalmia: Insights from an Egyptian cohort.
Journal: Molecular vision
Published: August 19, 2025
Lessons learned from the exome sequencing of nine cases of infertility and the way forward.
Journal: Reproductive biomedicine online
Published: July 28, 2025
Expanding the phenotype associated with biallelic SCNM1 variants.
Journal: Human genomics
Published: July 24, 2025
KREMEN1 Variants Associated with Ectodermal Dysplasia Impair Complex Formation of KREMEN1 with DKK1 and LRP6 and Attenuate WNT3A Response.
Journal: The Journal of investigative dermatology
Published: March 14, 2025
Analysis of Copy Number Variants Is an Important Consideration in Exome Sequencing.
Journal: Clinical genetics
Published: February 26, 2025
Last Updated: 09/26/2026