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Mutation Research|February 23, 2016
Identification of six novel mutations in Iranian patients with maple syrup urine disease and their in silico analysisMaryam Abiri, Razieh Karamzadeh, Morteza Karimipoor, et al.Hemoglobin|July 27, 2007
Globin chain synthesis is a useful complementary tool in the differential diagnosis of thalassemiasShohreh Khatami, Soghra Rouhi Dehboneh, Sedigheh Sadeghi, et al.Epidemics|June 21, 2021
Lessons for preparedness and reasons for concern from the early COVID-19 epidemic in IranMahan Ghafari, Bardia Hejazi, Arman Karshenas, et al.European Journal of Human Genetics : EJHG|September 7, 2017
Autosomal recessive congenital ichthyosis: CERS3 mutations identified by a next generation sequencing panel targeting ichthyosis genesLeila Youssefian, Hassan Vahidnezhad, Amir Hossein Saeidian, et al.JIMD Reports|May 27, 2015
Molecular Characterization of QDPR Gene in Iranian Families with BH4 Deficiency: Reporting Novel and Recurrent MutationsHannaneh Foroozani, Maryam Abiri, Shadab Salehpour, et al.Hepato-Gastroenterology|June 30, 2010
Three common CARD15 mutations are not responsible for the pathogenesis of Crohn's disease in IraniansLadan Teimoori-Toolabi, Homayoun Vahedi, Hamid Mollahajian, et al.Metabolic Brain Disease|August 11, 2016
In silico analysis of novel mutations in maple syrup urine disease patients from IranMaryam Abiri, Razieh Karamzadeh, Marziyeh Mojbafan, et al.Journal of Hepatology|April 8, 2019
Inherited non-alcoholic fatty liver disease and dyslipidemia due to monoallelic ABHD5 mutationsLeila Youssefian, Hassan Vahidnezhad, Amir Hossein Saeidian, et al.Frontiers in Genetics|June 5, 2023
Genetic attributes of Iranian cystic fibrosis patients: the diagnostic efficiency of CFTR mutations in over a decadeAmin Hosseini Nami, Mahboubeh Kabiri, Fatemeh Zafarghandi Motlagh, et al.Archives of Iranian Medicine|October 8, 2013
Prenatal diagnosis of β-thalassemia in twin pregnancies in IranZahra Kainimoghaddam, Atefeh Valaei, Fatemeh Bayat, et al.Pageof 18