A Multiplex Allele Specific Polymerase Chain Reaction (MAS-PCR) for the Detection of Factor V Leiden and Prothrombin G20210A

Por Bagheri, Morteza, Rad, Isa Abdi
Publicado em 2011

Analysis of the Most Common Three MEFV Mutations in 630 Patients with Familial Mediterranean Fever in Iranian Azeri Turkish Population

Por BAGHERI, Morteza, RAD, Isa Abdi
Publicado no Maedica (Bucur) (2017)

Molecular Evaluation of the IFN γ +874, TNF α -308, and IL-1Ra VNTR Sequences in Silicosis

Por RAD, Isa Abdi, MOHEBBI, Iraj, BAGHERI, Morteza
Publicado em 2012

A Case Report of 9p Deletion Syndrome Associated with Partial Trisomy of 1q42

Por VAHABI, Ali, HAZAN, Filiz, RAD, Isa Abdi
Publicado no Maedica (Bucur) (2017)

Lack of Association of Vitamin D Receptor FokI (rs10735810) (C/T) and BsmI (rs1544410) (A/G) Genetic Variations with Polycystic Ovary Syndrome Risk: a Case-control Study from Irani...

Por BAGHERI, Morteza, RAD, Isa Abdi, JAZANI, Nima Hosseini, NANBAKHSH, Fariba
Publicado em 2012

Association Between PAH Mutations and VNTR Alleles in the West Azerbaijani PKU Patients

Por BAGHERI, Morteza, RAD, Isa Abdi, JAZANI, Nima Hosseini, ZARRIN, Rasoul, GHAZAVI, Ahad
Publicado no Maedica (Bucur) (2014)

Mutation analysis of the phenylalanine hydroxylase gene in Azerbaijani population, a report from West Azerbaijan province of Iran

Por Bagheri, Morteza, Rad, Isa Abdi, Jazani, Nima Hosseini, Zarrin, Rasoul, Ghazavi, Ahad
Publicado no Iran J Basic Med Sci (2015)

Frequency of the VNTR-Polymorphisms at the PAH Gene in the Iranian Azeri Turkish Patients with Phenylketonuria

Por Bagheri, Morteza, Rad, Isa Abdi, Jazani, Nima Hosseini, Zarrin, Rasoul, Ghazavi, Ahad
Publicado no Maedica (Bucur) (2015)