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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.Matrix Biology : Journal of the International Society for Matrix Biology|May 18, 2021
Kindler epidermolysis bullosa-like skin phenotype and downregulated basement membrane zone gene expression in poikiloderma with neutropenia and a homozygous USB1 mutationHassan Vahidnezhad, Leila Youssefian, Amir Hossein Saeidian, et al.Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|February 20, 2019
Inherited Interleukin 2-Inducible T-Cell (ITK) Kinase Deficiency in Siblings With Epidermodysplasia Verruciformis and Hodgkin LymphomaLeila Youssefian, Hassan Vahidnezhad, Mehdi Yousefi, 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.Matrix Biology : Journal of the International Society for Matrix Biology|November 22, 2018
Mutations in PLOD3, encoding lysyl hydroxylase 3, cause a complex connective tissue disorder including recessive dystrophic epidermolysis bullosa-like blistering phenotype with abnormal anchoring fibrils and type VII collagen deficiencyHassan Vahidnezhad, Leila Youssefian, Amir Hossein Saeidian, et al.Pageof 2