Farah Talebi

发表

Novel LDB3 Mutation in a Patient With Autosomal Dominant Myofibrillar Myopathy

J. Asl, F. Ghanbari, Farah Talebi, 2016 .

A Novel Deletion Mutation of the TYR Gene in a Patient With Oculocutaneous Albinism Type 1A

J. Asl, F. Ghanbari, Farah Talebi, 2016 .

Identification of a Novel Non-Stop Mutation in PDE6C Gene in an Iranian Family With Con-Rod Dystrophy

S. Nasiri, J. Asl, F. Mardasi, 2020, ACTA MEDICA IRANICA.

Mutational spectrum of the CYP1B1 gene in Iranain primary congenital glaucoma family.

J. Asl, F. Mardasi, Farah Talebi, 2017, Canadian journal of ophthalmology. Journal canadien d'ophtalmologie.

Frequency of GJB2 mutations in families with autosomal recessive non-syndromic hearing loss in Khuzestan province

N. Saki, Ladan Sadeghian, J. Mohammadi-Asl, 2018 .

Next-generation sequencing identifies three novel missense variants in ILDR1 and MYO6 genes in an Iranian family with hearing loss with review of the literature.

J. Asl, Masoomeh Sayahi, F. Mardasi, 2017, International journal of pediatric otorhinolaryngology.

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

J. Mohammadi Asl, Farah Talebi, Farideh Ghanbari Mardasi, 2018, Cell journal.

Digenic Mutations in Junctional Epidermolysis Bullosa in An Iranian Family

J. Mohammadi Asl, K. Riahi, Farah Talebi, 2021, Cell journal.

Novel Homozygous Mutation in the MYO15A Gene in Autosomal Recessive Hearing Loss

J. Asl, F. Mardasi, Farah Talebi, 2016 .

Next-Generation Sequencing Reveals One Novel Missense Mutation in COL1A2 Gene in an Iranian Family with Osteogenesis imperfecta

J. Asl, F. Mardasi, A. Bavarsad, 2017, Iranian biomedical journal.

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

J. Mohammadi Asl, Farah Talebi, A. Lashgari, 2018, Cell journal.