Soumaya Zerelli-Mougou

Common Service Unit In Genetics
Sousse, Tunisia

Last Updated: 09/26/2026

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Found 26 publications

Comprehensive analysis of copy number variations in congenital heart defects Tunisian patients: chromosomal microarray analysis insights.

Comprehensive analysis of copy number variations in congenital heart defects Tunisian patients: chromosomal microarray analysis insights.

Journal: Molecular cytogenetics

Published: December 01, 2025

Why publish? Perspectives of North African researchers in the medical field.

Why publish? Perspectives of North African researchers in the medical field.

Journal: La Tunisie medicale

Published: April 20, 2025

Genetic investigation of the ubiquitin-protein ligase E3A gene as putative target in Angelman syndrome.

Genetic investigation of the ubiquitin-protein ligase E3A gene as putative target in Angelman syndrome.

Journal: World journal of clinical cases

Published: October 31, 2023

Bloom syndrome in children: unusual case of early onset lung damage.

Bloom syndrome in children: unusual case of early onset lung damage.

Journal: Clinical dysmorphology

Published: March 06, 2023

Case report: 7p22.3 deletion and 8q24.3 duplication in a patient with epilepsy and psychomotor delay-Does both possibly act to modulate a candidate gene region for the patient's phenotype?

Case report: 7p22.3 deletion and 8q24.3 duplication in a patient with epilepsy and psychomotor delay-Does both possibly act to modulate a candidate gene region for the patient's phenotype?

Journal: Frontiers in genetics

Published: October 04, 2022

Anomalies in Human Sex Determination: Usefulness of a Combined Cytogenetic Approach to Characterize an Additional Case with Xp Functional Disomy Associated with 46,XY Gonadal Dysgenesis

Anomalies in Human Sex Determination: Usefulness of a Combined Cytogenetic Approach to Characterize an Additional Case with Xp Functional Disomy Associated with 46,XY Gonadal Dysgenesis

Journal: Journal of clinical research in pediatric endocrinology

Published: August 19, 2022

Clinical and molecular characterization of 1q43q44 deletion and corpus callosum malformations: 2 new cases and literature review.

Clinical and molecular characterization of 1q43q44 deletion and corpus callosum malformations: 2 new cases and literature review.

Journal: Molecular cytogenetics

Published: August 01, 2022

Additional evidence for the role of chromosomal imbalances and SOX8, ZNRF3 and HHAT gene variants in early human testis development.

Additional evidence for the role of chromosomal imbalances and SOX8, ZNRF3 and HHAT gene variants in early human testis development.

Journal: Reproductive biology and endocrinology : RB&E

Published: July 14, 2022

Further report of MEDS syndrome: Clinical and molecular delineation of a new Tunisian case.

Further report of MEDS syndrome: Clinical and molecular delineation of a new Tunisian case.

Journal: European journal of medical genetics

Published: March 12, 2021

Disorders of sex development in Wolf-Hirschhorn syndrome: a genotype-phenotype correlation and MSX1 as candidate gene.

Disorders of sex development in Wolf-Hirschhorn syndrome: a genotype-phenotype correlation and MSX1 as candidate gene.

Journal: Molecular cytogenetics

Published: December 23, 2020

Small supernumerary marker chromosomes (sSMC) and male infertility: characterization of five new cases, review of the literature, and perspectives.

Small supernumerary marker chromosomes (sSMC) and male infertility: characterization of five new cases, review of the literature, and perspectives.

Journal: Journal of assisted reproduction and genetics

Published: January 11, 2020

Neuronal migration genes and a familial translocation t (3;17): candidate genes implicated in the phenotype.

Neuronal migration genes and a familial translocation t (3;17): candidate genes implicated in the phenotype.

Journal: BMC medical genetics

Published: June 20, 2019

Showing 1-12 of 26

Last Updated: 09/26/2026