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Author = Maryam Hajilari

Number of Articles: 2
Frequency of c.35delG Mutation in GJB2 gene in Patients with Autosomal Recessive Non-Syndromic Hearing Loss of Five Ethnic Groups in Golestan, Iran
Frequency of c.35delG Mutation in GJB2 gene in Patients with Autosomal Recessive Non-Syndromic Hearing Loss of Five Ethnic Groups in Golestan, Iran

Maryam Hajilari; Atefeh Sharifinya; Teymoor Khosravi; Anvarsadat Kianmehr; Mohammad Hossein Taziki; Ayyoob Khosravi; Morteza Oladnabi

Volume 11, Issue 1 , January 2023, , Pages 17286-17298

https://doi.org/10.22038/ijp.2023.69158.5122

Abstract
  Background: Hereditary Hearing Loss (HL) is one of the most prevalent sensorineural disorders worldwide. Several hundreds of genes have been reported to have associations with this ...  Read More
Hereditary Hearing Loss and Consanguinity in Turkmen Population of Iran: A Retrospective Study
Hereditary Hearing Loss and Consanguinity in Turkmen Population of Iran: A Retrospective Study

Maryam Hajilari; Morteza Oladnabi; Anvarsadat Kianmehr; Mohammad Hossein Taziki; Farzaneh Zamiri Abdollahi

Volume 7, Issue 11 , November 2019, , Pages 10323-10334

https://doi.org/10.22038/ijp.2019.41740.3519

Abstract
  Background: Our research focuses on different dimensions of families of Turkmen population of Iran with two or more than two affected members. A complete clinical ear test was conducted ...  Read More