The proportion of tetrahydrobiopterin deficiency and PAH gene deficiency variants among cases with hyperphenyalaninemia in Western Iran

por Moradi, Keyvan, Alibakhshi, Reza, Khatami, Shohreh
Publicado 2013

CFTR Mutation Analysis in Western Iran: Identification of Two Novel Mutations

por Karimi, Nasibeh, Alibakhshi, Reza, Almasi, Shekoufeh
Publicado 2018

The status of PAH gene-VNTR alleles and mini-haplotypes associations with PAH gene mutations in Iranian Kurdish PKU patients

por Alibakhshi, Reza, Moradi, Keivan, Ghadiri, Keyghobad
Publicado 2019

Mutation Analysis of Exons 10 and 17a of CFTR Gene in Patients with Cystic Fibrosis in Kermanshah Province, Western Iran

por Sahami, Abbas, Alibakhshi, Reza, Ghadiri, Keyghobad, Sadeghi, Hamid
Publicado 2014

Spectrum of Phenylalanine Hydroxylase Gene Mutations in Hamadan and Lorestan Provinces of Iran and Their Associations with Variable Number of Tandem Repeat Alleles

por Alibakhshi, Reza, Moradi, Keivan, Biglari, Mostafa, Shafieenia, Samaneh
Publicado 2018

Molecular analysis of exons 6 and 7 of phenylalanine hydroxylase gene mutations in Phenylketonuria patients in Western Iran

por Moradi, Keyvan, Alibakhshi, Reza, Ghadiri, Keyghobad, Khatami, Saeid Reza, Galehdari, Hamid
Publicado 2012

Cytogenetic Analysis of 570 Couples with Recurrent Pregnancy Loss: Reporting 11 Years of Experience

por Alibakhshi, Reza, Nejati, Parham, Hamani, Sara, Mir-Ahadi, Narges, Jalilian, Nazanin
Publicado 2020

Aberrant Methylation of APAF-1 Gene in Acute Myeloid Leukemia Patients

por Rostami, Shahrbano, Nadali, Fatemeh, Alibakhshi, Reza, Zaker, Farhad, Nasiri, Nahid, Payandeh, Mehrdad, Chahardouli, Bahram, Maleki, Ali
Publicado 2017

Reporting a novel growth hormone receptor gene variant in an Iranian consanguineous pedigree with Laron syndrome: a case report

por Bitarafan, Fatemeh, Khodaeian, Mehrnoosh, Garrousi, Fatemeh, Khalesi, Raziyeh, Ghazi Nader, Donya, Karimi, Behnam, Alibakhshi, Reza, Garshasbi, Masoud
Publicado 2023