P. Tahmasebi

A novel pathogenic variant in the MARVELD2 gene causes autosomal recessive non-syndromic hearing loss in an Iranian family.

N. Saki, M. Tabatabaiefar, M. Hashemzadeh-Chaleshtori, 2019, Genomics.

A Patient with Trisomy 4 p and Monosomy 10 q

P. Tahmasebi, M. Sobhani, F. Nasiri, 2019 .

Rapid identification of extensively and extremely drug resistant tuberculosis from multidrug resistant strains; using PCR-RFLP and PCR-SSCP

A. Velayati, P. Tahmasebi, P. Farnia, 2012, Iranian journal of microbiology.

A Novel Pathologic Variant in OTOF in an Iranian Family Segregating Hereditary Hearing Loss

R. Salehi, N. Saki, M. Tabatabaiefar, 2018, Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.

Prevalence of Urinary Tract Infection and Associated Risk Factors in Pregnant Women

F. Pourfarzi, S. Moradi, P. Tahmasebi, 2014 .

An Overview of Hereditary Diseases in Khuzestan Province, Southwest Iran

P. Tahmasebi, S. K. Nezhad, 2015 .

A novel TECTA mutation causes ARNSHL.

M. Ghahremani, M. Modarressi, M. Tabatabaiefar, 2017, International journal of pediatric otorhinolaryngology.

Next-generation sequencing reveals a novel pathological mutation in the TMC1 gene causing autosomal recessive non-syndromic hearing loss in an Iranian kindred.

Ladan Sadeghian, M. Tabatabaiefar, P. Tahmasebi, 2019, International journal of pediatric otorhinolaryngology.

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

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

Genetic Linkage Analysis of DFNB2 Locus with Autosomal Recessive Hearing Loss in Families Negative for GJB2 Mutations in Khuzestan Province

N. Saki, J. Asl, M. Tabatabaiefar, 2016 .

Genetic Linkage Analysis of the DFNB21 Locus in Autosomal Recessive Hearing Loss in large families from Khuzestan Province.

E. Asgari, N. Saki, R. Ghasemikhah, 2017 .