Volume 12 (2024)
Volume 11 (2023)
Volume 10 (2022)
Volume 9 (2021)
Volume 8 (2020)
Volume 7 (2019)
Volume 6 (2018)
Volume 5 (2017)
Volume 4 (2016)
Volume 3 (2015)
Volume 2 (2014)
Volume 1 (2013)
Prevalence of Cystic Fibrosis Trans-membrane Conductance Regulator Gene common mutations in children with cystic fibrosis in Isfahan, Iran
Prevalence of Cystic Fibrosis Trans-membrane Conductance Regulator Gene common mutations in children with cystic fibrosis in Isfahan, Iran

Mohsen Reisi; Mahdiyeh Behnam; Seyed Javad Sayedi; Farzaneh Salimi; Pegah Kargar; Mansoor Salehi; Hossein Saneian; Iman Kashani; Roya Kelishadi

Volume 7, Issue 4 , April 2019, , Pages 9333-9339

https://doi.org/10.22038/ijp.2018.36309.3168

Abstract
  Background: Cystic fibrosis (CF) is the most common lethal genetic disorder of Cystic Fibrosis Trans-membrane Conductance (CFTR) Regulator gene mutations. We aimed to investigate common ...  Read More
Evaluation of GJB2 and GJB6 Mutations in Patients Afflicted with Non-syndromic Hearing Loss
Evaluation of GJB2 and GJB6 Mutations in Patients Afflicted with Non-syndromic Hearing Loss

Seyed Hamid Reza Abtahi; Ali Malekzadeh; Saeed Soheilipour; Mansour Salehi; Roya Taleban; Reyhaneh Rabieian; Mohammad Moafi

Volume 7, Issue 2 , February 2019, , Pages 9053-9060

https://doi.org/10.22038/ijp.2018.34154.3017

Abstract
  Background Non-syndromic hearing loss (NSHL) is assumed as one of the highly prevalent congenital defects in the world. In this regard, gap junction protein beta 2(GJB2), and gap junction ...  Read More