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Blood Reviews|July 26, 2016
Beta thalassemia in 31,734 cases with HBB gene mutations: Pathogenic and structural analysis of the common mutations; Iran as the crossroads of the Middle EastNejat Mahdieh, Bahareh RabbaniIranian Journal of Pediatrics|January 16, 2014
An overview of mutation detection methods in genetic disordersNejat Mahdieh, Bahareh RabbaniClinical Case Reports|February 18, 2021
HBB mutations and HbA2 level: Escaping the carrier screening programsAmeneh Sharifi, Nejat MahdiehInternational Journal of Audiology|November 21, 2009
Statistical study of 35delG mutation of GJB2 gene: a meta-analysis of carrier frequencyNejat Mahdieh, Bahareh RabbaniJournal of Cardiovascular and Thoracic Research|December 12, 2019
A comprehensive in silico analysis, distribution and frequency of human Nkx2-5 mutations; A critical gene in congenital heart diseaseSamira Kalayinia, Serwa Ghasemi, Nejat MahdiehAtherosclerosis|July 7, 2020
A systematic review of LDLR, PCSK9, and APOB variants in AsiaNejat Mahdieh, Katayoun Heshmatzad, Bahareh RabbaniJournal of Human Genetics|November 8, 2013
The promise of whole-exome sequencing in medical geneticsBahareh Rabbani, Mustafa Tekin, Nejat MahdiehAnnals of Medicine|October 14, 2017
Next generation sequencing applications for cardiovascular diseaseSamira Kalayinia, Hamidreza Goodarzynejad, Majid Maleki, et al.European Journal of Medical Research|September 26, 2023
TCAP gene is not a common cause of cardiomyopathy in Iranian patientsZahra Alaei, Nasrin Zamani, Bahareh Rabbani, et al.Journal of Clinical Laboratory Analysis|December 24, 2019
A novel de novo dominant mutation of NOTCH1 gene in an Iranian family with non-syndromic congenital heart diseaseSamira Kalayinia, Majid Maleki, Mohammad Mahdavi, et al.Pageof 10