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Biochemical and Biophysical Research Communications|May 8, 2016
Mutational screening in patients with profound sensorineural hearing loss and neurodevelopmental delay: Description of a novel m.3861A > C mitochondrial mutation in the MT-ND1 geneMarwa Ammar, Mouna Tabebi, Lamia Sfaihi, et al.Biochemical and Biophysical Research Communications|March 20, 2016
Mutational analysis in patients with neuromuscular disorders: Detection of mitochondrial deletion and double mutations in the MT-ATP6 geneRahma Felhi, Emna Mkaouar-Rebai, Lamia Sfaihi-Ben Mansour, et al.Biochemical and Biophysical Research Communications|February 22, 2015
A novel mutation MT-COIII m.9267G>C and MT-COI m.5913G>A mutation in mitochondrial genes in a Tunisian family with maternally inherited diabetes and deafness (MIDD) associated with severe nephropathyMouna Tabebi, Emna Mkaouar-Rebai, Mouna Mnif, et al.Gene|October 9, 2017
Association study of apoptosis gene polymorphisms in mitochondrial diabetes: A potential role in the pathogenicity of MDMouna Tabebi, Bodour Khabou, Hanen Boukadi, et al.Biochemical and Biophysical Research Communications|March 30, 2018
A novel TBX1 missense mutation in patients with syndromic congenital heart defectsAmel Jaouadi, Mouna Tabebi, Fatma Abdelhedi, et al.Frontiers in Endocrinology|November 28, 2022
Case report: Two sisters with a germline CHEK2 variant and distinct endocrine neoplasiasRaphaelle D Vallera, Yanli Ding, Kimmo J Hatanpaa, et al.Pageof 3