Sameh M. Senousy
Cairo, C, Egypt
Last Updated: 09/26/2026
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Found 8 publications
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
Evaluating microRNA-720 and microRNA-1275 as Noninvasive Specific Test Compared With Maternal Serum Alpha-Fetoprotein and Three-Dimensional Ultrasound to Diagnose Fetal Neural Tube Defects.
Journal: The journal of obstetrics and gynaecology research
Published: February 09, 2026
Analysis of Copy Number Variants Is an Important Consideration in Exome Sequencing.
Journal: Clinical genetics
Published: February 26, 2025
Integrating Prenatal Exome Sequencing and Ultrasonographic Fetal Phenotyping for Assessment of Congenital Malformations: High Molecular Diagnostic Yield and Novel Phenotypic Expansions in a Consanguineous Cohort.
Journal: Clinical genetics
Published: November 02, 2024
Lethal Phenotype and Expansion of the Clinical Spectrum of Biallelic Loss of Function Variant in SENP7 Gene Unveiled by Whole Exome Sequencing.
Journal: Clinical genetics
Published: October 23, 2024
Fetal Phenotyping and Whole Exome Sequencing for 12 Egyptian Families With Serine Biosynthesis Defect: Novel Clinical and Allelic Findings With a Founder Effect.
Journal: Prenatal diagnosis
Published: July 23, 2024
Association between biomarkers of vitamin B12 status and the risk of neural tube defects.
Journal: The journal of obstetrics and gynaecology research
Published: March 23, 2018
Showing 1-8 of 8
Last Updated: 09/26/2026