Hajer Foddha
Monastir, Tunisia
Last Updated: 09/26/2026
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Found 8 publications
Comprehensive analysis of a novel LYST mutation in a Tunisian patient with Chediak-Higashi syndrome.
Comprehensive analysis of a novel LYST mutation in a Tunisian patient with Chediak-Higashi syndrome.
Journal: BMC medical genomics
Published: February 24, 2025
Utility of regional STR marker variations in Tunisian and sub-Saharan populations: insights into forensic and population genetics.
Journal: Frontiers in bioinformatics
Published: January 11, 2025
Genetic variations in the IDUA gene in Tunisian MPS I families: Identification of a novel microdeletion disrupting substrate binding and structural insights.
Journal: Molecular genetics and metabolism reports
Published: October 15, 2024
Analysis of genetic polymorphisms and mRNA expression of DRD3 and HTR2A in bruxism.
Journal: BMC oral health
Published: September 28, 2024
Involvement of CXCL10 rs4256246, CXCR4 rs2228014, CCR2 rs1799864 and CXCL16 rs2277680 in the Predisposition to Schizophrenia.
Journal: Journal of molecular neuroscience : MN
Published: March 21, 2024
The association between Dental Fluorosis and COL1A2 gene polymorphism among a Tunisian Population.
Journal: BMC oral health
Published: November 30, 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
Single nucleotide polymorphisms of SCN5A and SCN10A genes increase the risk of ventricular arrhythmias during myocardial infarction.
Journal: Advances in clinical and experimental medicine : official organ Wroclaw Medical University
Published: April 25, 2020
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Last Updated: 09/26/2026