Molecular Analysis of rs2070744 and rs1799983 Polymorphisms of NOS3 Gene in Iranian Patients With Multiple Sclerosis by Mohammad Mehdi Heidari, Mehri Khatami, Yaser Tahamtan

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Review of Genetic Changes and Factors Causing Cardiac Arrhythmias by Mehri Khatami, Mohammad Mehdi Heidari, Bahareh Mazrouei, Rojin Aflaki

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Studying the Pathogenic Effect of New Nucleotide Changes in the Promoter Region of the TERT Gene in Patients with Glioblastoma Brain Tumor by Farzaneh Owlia, Mohammad Mehdi Heidari, Mehri Khatami, Ehsan Ziaei, Mohammad Ali Broomand

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Genomic and bioinformatics analysis of nucleotide changes in the coding regions of the CCDC103 gene in patients with Tetralogy of Fallot (TOF): A type of Congenital Heart Defects by Zahra Moghadambarati, Mehri Khatami, Mohammad Mehdi Heidari, Mehdi HadadZadeh, Reihane Ghorbanian

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Genetic Causes of Familial Adenomatous Polyposis (FAP), Risk Factors and Clinical Outcomes by Mohammad Mehdi Heidari, Elham Afkhami aqhda, Maryam Tahmasebi, Mehri Khatami, Zahra Shaker Ardakani

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Molecular Study of Nucleotide Changes of ATPase6 and MT-CYB Genes in the Mitochondrial Genome of Patients with Familial Adenomatous Polyposis (FAP) by Mohammad Mehdi Heidari, Fatemeh Ebrahimi, Zahra Shaker Ardakani, Mahsa Mirzaei, Shima Mirhosseini, Mehri Khatami

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Mitochondrial mutations in protein coding genes of respiratory chain including complexes IV, V, and mt-tRNA genes are associated risk factors for congenital heart disease by Mohammad Mehdi Heidari, Mehri Khatami, Akram Kamalipour, Mustafa Kalantari, Mahsa Movahed, Mohammad Hayet Emmamy, Mehdi Hadadzadeh, José Bragança, Mohsen Namnabat, Bahareh Mazrouei

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