Identification of A Novel Missense Mutation in The Norrie Disease Gene: The First Molecular Genetic Analysis and Prenatal Diagnosis of Norrie Disease in An Iranian Family

por Talebi, Farah, Ghanbari Mardasi, Farideh, Mohammadi Asl, Javad, Lashgari, Ali, Farhadi, Freidoon
Publicado 2018

Identification of a Novel WFS1 Mutation Using the Whole Exome Sequencing in an Iranian Pedigree with Autosomal Dominant Hearing Loss

por Mohammadi-asl, Javad, Saki, Nader, Dehdashtiyan, Masoud, Neissi, Mostafa, Ghanbari Mardasi, Farideh
Publicado 2021

Digenic Mutations in Junctional Epidermolysis Bullosa in An Iranian Family

por Riahi, Kourosh, Ghanbari Mardasi, Farideh, Talebi, Farah, Jasemi, Farzad, Mohammadi Asl, Javad
Publicado 2021

Identification of Novel PTPRQ and MYO1A Mutations in An Iranian Pedigree with Autosomal Recessive Hearing Loss

por Talebi, Farah, Ghanbari Mardasi, Farideh, Mohammadi Asl, Javad, Tizno, Saeed, Najafvand Zadeh, Marziye
Publicado 2018

Association of human leukocyte antigen-DRB haplotype in multiple sclerosis population of Khuzestan, Iran

por Delfan, Nooshin, Galehdari, Hamid, Shafiei, Mohammad, Ghanbari-Mardasi, Farideh, Latifi, Tahereh, Majdinasab, Nastaran, Seifi, Tahereh
Publicado 2018

Association of HLA-DR2-Related Haplotype (HLA-DRB5*01-DRB1*1501-DQB1*0602) in Patients with Multiple Sclerosis in Khuzestan Province

por DELFAN, Nooshin, GALEHDARI, Hamid, GHANBARI MARDASI, Farideh, ZABIHI, Rezvan, LATIFI PAKDEHI, Tahereh, SEIFI, Tahereh, MAJDINASAB, Nastaran
Publicado 2021