Author:
Asgharzade Samira,Tabatabaiefar Mohammad Amin,Modarressi Mohammad Hossein,Ghahremani Mohammad Hossein,Reiisi Somayeh,Tahmasebi Parisa,Abdollahnejad Fatemeh,Chaleshtori Morteza Hashemzadeh
Funder
Tehran University of Medical Sciences
Ahvaz Jundishapur University of Medical Sciences
Shahrekord University of Medical Sciences
Subject
Otorhinolaryngology,General Medicine,Pediatrics, Perinatology and Child Health
Reference26 articles.
1. Mutations in the second exon of MYO15Agene causes of nonsyndromic hearing loss and its association in the Arab population in Iran;Asgharzade;Genetika,2016
2. Genetic counseling for patients with nonsyndromic hearing impairment directed by gene analysis;Ma;Mol. Med. Rep.,2016
3. Human nonsyndromic sensorineural deafness, nnu;Friedman;Rev. Genomics Hum. Genet.,2003
4. Hereditary Hearing Loss Homepage. Definitions, Protocols and Guidelines in Genetic Hearing Impairment;Van Camp,2003
5. The study of SLC26A4 gene causing autosomal recessive hearing loss by linkage analysis in a cohort of iranian populations;Reiisi;Int. J. Mol. Cell. Med.,2014
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