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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 RabbaniInternational Journal of Audiology|November 21, 2009
Statistical study of 35delG mutation of GJB2 gene: a meta-analysis of carrier frequencyNejat Mahdieh, Bahareh RabbaniAtherosclerosis|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 MahdiehEuropean 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.Molecular Biosystems|April 13, 2016
Next generation sequencing: implications in personalized medicine and pharmacogenomicsBahareh Rabbani, Hirofumi Nakaoka, Shahin Akhondzadeh, et al.International Journal of Endocrinology|September 21, 2020
The Genetic Perspective of Familial Glucocorticoid Deficiency: In Silico Analysis of Two Novel VariantsKatayoun Heshmatzad, Nejat Mahdieh, Ali Rabbani, et al.Journal of Human Genetics|July 27, 2012
Next-generation sequencing: impact of exome sequencing in characterizing Mendelian disordersBahareh Rabbani, Nejat Mahdieh, Kazuyoshi Hosomichi, et al.Clinical Case Reports|October 22, 2020
A novel pathogenic variant of SRD5A2 in an Iranian psuedohermaphrodite maleSetilla Dalili, Bahareh Rabbani, Afagh Hassanzadeh Rad, et al.Pageof 10