Last Updated: 09/26/2026
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Found 100 publications
Comprehensive analysis of copy number variations in congenital heart defects Tunisian patients: chromosomal microarray analysis insights.
Journal: Molecular cytogenetics
Published: December 01, 2025
Genetic Insights Into Epidermolysis Bullosa: Identification of Novel Variants in Tunisian Patients.
Journal: American journal of medical genetics. Part A
Published: May 15, 2024
RS35705950 polymorphism of MUC5B Gene: Association with Rheumatoid Arthritis and Interstitial lung disease in Tunisian Population.
Journal: La Tunisie medicale
Published: April 17, 2024
Functional analysis of MMR gene VUS from potential Lynch syndrome patients.
Journal: PloS one
Published: November 03, 2023
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
Is Tunisia ready for precision medicine? Challenges of medical genomics within a LMIC healthcare system.
Journal: Journal of community genetics
Published: September 22, 2023
Nuclear sperm integrity and ICSI prognosis in Tunisian patients with MMAF syndrome (multiple morphological abnormalities of the sperm flagella).
Journal: Human fertility (Cambridge, England)
Published: September 06, 2023
Response to growth hormone therapy in ring chromosome 15: Review and evidence from a new case on possible beneficial effect in neurodevelopment.
Journal: Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society
Published: May 27, 2023
Genome Tunisia Project: paving the way for precision medicine in North Africa.
Journal: Genome medicine
Published: May 02, 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?
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
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.
Journal: Molecular cytogenetics
Published: August 01, 2022
Last Updated: 09/26/2026