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Scientific Reports|May 17, 2019
Development and validation of a novel panel of 16 STR markers for simultaneous diagnosis of β-thalassemia, aneuploidy screening, maternal cell contamination detection and fetal sample authenticity in PND and PGD/PGS casesZohreh Sharifi, Faezeh Rahiminejad, Atefeh Joudaki, et al.The Journal of Investigative Dermatology|November 26, 2016
Gene-Targeted Next Generation Sequencing Identifies PNPLA1 Mutations in Patients with a Phenotypic Spectrum of Autosomal Recessive Congenital Ichthyosis: The Impact of ConsanguinityHassan Vahidnezhad, Leila Youssefian, Amir Hossein Saeidian, et al.Journal of Molecular Neuroscience : MN|January 22, 2021
Comprehensive Mutation Analysis and Report of 12 Novel Mutations in a Cohort of Patients with Spinal Muscular Atrophy in IranZohreh Sharifi, Mohammad Taheri, Mohammad-Sadegh Fallah, et al.Matrix Biology : Journal of the International Society for Matrix Biology|November 16, 2017
Recessive mutation in tetraspanin CD151 causes Kindler syndrome-like epidermolysis bullosa with multi-systemic manifestations including nephropathyHassan Vahidnezhad, Leila Youssefian, Amir Hossein Saeidian, et al.Experimental Dermatology|January 25, 2018
Genome-wide single nucleotide polymorphism-based autozygosity mapping facilitates identification of mutations in consanguineous families with epidermolysis bullosaHassan Vahidnezhad, Leila Youssefian, Amir Hossein Saeidian, et al.Journal of Inherited Metabolic Disease|August 31, 2018
Molecular genetics of a cohort of 635 cases of phenylketonuria in a consanguineous populationTina Shirzadeh, Amir Hossein Saeidian, Hamideh Bagherian, et al.Pageof 3