Molka Kammoun
Sousse, Tunisia
Last Updated: 09/26/2026
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Found 12 publications
Comprehensive analysis of copy number variations in congenital heart defects Tunisian patients: chromosomal microarray analysis insights.
Journal: Molecular cytogenetics
Published: December 01, 2025
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.
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.
Journal: European journal of medical genetics
Published: March 12, 2021
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.
Journal: Andrologia
Published: October 24, 2017
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.
Journal: Journal of pediatric genetics
Published: February 06, 2017
NOBOX is a strong autosomal candidate gene in Tunisian patients with primary ovarian insufficiency.
Journal: Clinical genetics
Published: December 28, 2015
Novel homozygous nonsense mutations in the luteinizing hormone receptor (LHCGR) gene associated with 46,XY primary amenorrhea.
Journal: Fertility and sterility
Published: August 31, 2015
Relationship between sperm aneuploidy, sperm DNA integrity, chromatin packaging, traditional semen parameters, and recurrent pregnancy loss.
Journal: Fertility and sterility
Published: June 27, 2015
Microarray Analysis of 8p23.1 Deletion in New Patients with Atypical Phenotypical Traits.
Journal: Journal of pediatric genetics
Published: April 01, 2015
Showing 1-12 of 12
Last Updated: 09/26/2026