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Journal of Pediatric Genetics|September 15, 2016
Molecular cytogenetic and phenotypic characterization of ring chromosome 13 in three unrelated patientsInesse B Abdallah-Bouhjar, Soumaya Mougou-Zerelli, Hanene Hannachi, et al.BMC Medical Genetics|February 8, 2020
Neuronal migration genes and a familial translocation t (3;17): candidate genes implicated in the phenotypeMeriam Hadj Amor, Sarra Dimassi, Amel Taj, et al.Molecular Cytogenetics|October 3, 2022
Clinical and molecular characterization of 1q43q44 deletion and corpus callosum malformations: 2 new cases and literature reviewBochra Khadija, Khouloud Rjiba, Sarra Dimassi, et al.American Journal of Medical Genetics. Part A|June 1, 2011
Array-CGH study of partial trisomy 9p without mental retardationInesse Ben Abdallah Bouhjar, Hanane Hannachi, Soumaya Mougou Zerelli, et al.Fertility and Sterility|March 27, 2016
Novel homozygous nonsense mutations in the luteinizing hormone receptor (LHCGR) gene associated with 46,XY primary amenorrheaImen Ben Hadj Hmida, Soumaya Mougou-Zerelli, Anis Hadded, et al.Fertility and Sterility|October 24, 2015
Relationship between sperm aneuploidy, sperm DNA integrity, chromatin packaging, traditional semen parameters, and recurrent pregnancy lossInes Zidi-Jrah, Amani Hajlaoui, Soumaya Mougou-Zerelli, et al.Journal of Assisted Reproduction and Genetics|May 14, 2020
Small supernumerary marker chromosomes (sSMC) and male infertility: characterization of five new cases, review of the literature, and perspectivesWafa Slimani, Afef Jelloul, Ahmed Al-Rikabi, et al.Journal of Clinical Research in Pediatric Endocrinology|August 19, 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 DysgenesisKhouloud Rjiba, Wafa Slimani, Meriem Gaddas, et al.Molecular Cytogenetics|February 19, 2019
Clinical and molecular findings in nine new cases of tetrasomy 18p syndrome: FISH and array CGH characterizationWafa Slimani, Hela Ben Khelifa, Sarra Dimassi, et al.World Journal of Clinical Cases|February 7, 2024
Genetic investigation of the ubiquitin-protein ligase E3A gene as putative target in Angelman syndromeWiem Manoubi, Marwa Mahdouani, Dorra Hmida, et al.Pageof 3