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Pediatric Neurology|December 15, 2010
Chromosomal microarray analysis in a girl with mental retardation and spina bifidaInesse Ben Abdallah, Hanene Hannachi, Najla Soyah, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 5, 2006
Rituximab in subacute sclerosing panencephalitisLuigi Titomanlio, Najla Soyah, Valérie Guerin, et al.
Journal of Pediatric Genetics|May 13, 2017
Genomic Microarray in Intellectual Disability: The Usefulness of Existing Systems in the Interpretation of Copy Number VariationHela Ben Khelifa, Najla Soyah, Audrey Labalme, et al.
European Journal of Medical Genetics|July 6, 2021
Further report of MEDS syndrome: Clinical and molecular delineation of a new Tunisian caseKhouloud Rjiba, Najla Soyah, Molka Kammoun, et al.
Journal of Pediatric Genetics|September 15, 2016
Trisomy and tetrasomy 15q11-q13 diagnosed by molecular cytogenetic analysis in two patients with mental retardationInesse Ben Abdallah Bouhjar, Abir Gmidène, Najla Soyah, et al.
Journal of Pediatric Genetics|September 13, 2016
Microarray Analysis of 8p23.1 Deletion in New Patients with Atypical Phenotypical TraitsHela Ben Khelifa, Molka Kammoun, Hanene Hannachi, et al.
Ear, Nose, & Throat Journal|May 19, 2026
Orbital Complications and Prognosis of Acute Ethmoiditis: A Pediatric Retrospective Observational StudyMarwa Abdelbari, Melek Mneri, Jihene Houas, et al.
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.
Gene|February 14, 2013
Phenotype and micro-array characterization of duplication 11q22.1-q25 and review of the literatureInesse Ben-Abdallah-Bouhjar, Soumya Mougou-Zerelli, Hanene Hannachi, et al.
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