Molecular genetic analysis of polycystic kidney disease 1 and polycystic kidney disease 2 mutations in pedigrees with autosomal dominant polycystic kidney disease

by Fatemeh Bitarafan, Masoud Garshasbi
Published 2019-01-01

The first case of NSHL by direct impression on EYA1 gene and identification of one novel mutation in MYO7A in the Iranian families

by Ehsan Razmara, Fatemeh Bitarafan, Elika Esmaeilzadeh-Gharehdaghi, Navid Almadani, Masoud Garshasbi
Published 2018-03-01

Three Novel Variants identified in FBN1 and TGFBR2 in seven Iranian families with suspected Marfan syndrome

by Fatemeh Bitarafan, Ehsan Razmara, Mehrnoosh Khodaeian, Mohammad Keramatipour, Alireza Kalhor, Ehsan Jafarinia, Masoud Garshasbi
Published 2020-08-01

A homozygote variant in the tRNA splicing endonuclease subunit 54 causes pontocerebellar hypoplasia in a consanguineous Iranian family

by Afrooz Sepahvand, Ehsan Razmara, Fatemeh Bitarafan, Mohammad Galehdari, Ali Reza Tavasoli, Navid Almadani, Masoud Garshasbi
Published 2020-10-01

Isolated Congenital Anosmia and CNGA2 Mutation

by M. Reza Sailani, Inlora Jingga, Seyed Hashem MirMazlomi, Fatemeh Bitarafan, Jonathan A. Bernstein, Michael P. Snyder, Masoud Garshasbi
Published 2017-06-01

Prevalence and Genotype Distribution of Human Papillomavirus Infection among 12 076 Iranian Women

by Fatemeh Bitarafan, Mohammad Reza Hekmat, Mehrnoosh Khodaeian, Ehsan Razmara, Tahereh Ashrafganjoei, Mitra Modares Gilani, Mitra Mohit, Soheila Aminimoghaddam, Fatemeh Cheraghi, Raziyeh Khalesi, Parnian Rajabzadeh, Soheila Sarmadi, Masoud Garshasbi
Published 2021-10-01