Wafa Slimani

Common Service Unit In Genetics
Sousse, Tunisia

Last Updated: 09/26/2026

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Found 10 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

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

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

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

Clinical and molecular findings in nine new cases of tetrasomy 18p syndrome: FISH and array CGH characterization.

Clinical and molecular findings in nine new cases of tetrasomy 18p syndrome: FISH and array CGH characterization.

Journal: Molecular cytogenetics

Published: November 20, 2018

Sperm fluorescent in situ hybridisation study of interchromosomal effect in six Tunisian carriers of reciprocal and Robertsonian translocations.

Sperm fluorescent in situ hybridisation study of interchromosomal effect in six Tunisian carriers of reciprocal and Robertsonian translocations.

Journal: Andrologia

Published: October 24, 2017

Subtelomeric Rearrangements in Patients with Recurrent Miscarriage.

Subtelomeric Rearrangements in Patients with Recurrent Miscarriage.

Journal: International journal of fertility & sterility

Published: March 17, 2017

Array Characterization of Prenatally Diagnosed 15q26 Microdeletion and 2q37.1 Duplication: Report of a New Case with Multicystic Kidneys and Review of the Literature.

Array Characterization of Prenatally Diagnosed 15q26 Microdeletion and 2q37.1 Duplication: Report of a New Case with Multicystic Kidneys and Review of the Literature.

Journal: Journal of pediatric genetics

Published: February 06, 2017

Showing 1-10 of 10

Last Updated: 09/26/2026