Strategies for whole-exome sequencing analysis in a case series study of familial male infertility

by Masomeh Askari, Dor Mohammad Kordi Tamandani, Navid Almadani, Mehdi Totonch
Published 2020-05-01

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

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