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Journal of Pediatric Genetics|September 15, 2016
Cytogenetic analysis in a large series of children with non-syndromic mental retardationInesse Ben Abdallah Bouhjar, Abir Gmidène, Soumaya Mougou-Zrelli, et al.La Tunisie Medicale|March 28, 2024
Cribriform plate dehiscence with encephalomeningocele revealed by recurrent meningitis: A case reportNajla Soyah, Hajer Ben Belgacem, Donia Brahem, et al.European Journal of Medical Genetics|June 12, 2012
Chromosomal microarray analysis of functional Xq27-qter disomy and deletion 3p26.3 in a boy with Prader-Willi like features and hypotoniaInesse Ben-Abdallah-Bouhjar, Hanene Hannachi, Audrey Labalme, 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.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.Hemoglobin|May 29, 2015
Multiplex Minisequencing of the HBB Gene: A Rapid Strategy to Confirm the Most Frequent β-Thalassemia Mutations in the Tunisian PopulationIlhem Ben Charfeddine, Taheni Ben Lazreg, Ahlem M'sakni, et al.Pageof 2