Repository of Research and Investigative Information
Ilam University of Medical Sciences
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(2014) The promise of whole-exome sequencing in medical genetics. Journal of Human Genetics. pp. 5-15. ISSN 1434-5161
(2013) Correction: Whole-exome sequencing efficiently detects rare mutations in autosomal recessive nonsyndromic hearing loss. (PLoS ONE). Plos One. ISSN 19326203 (ISSN)
(2012) Screening of OTOF mutations in Iran: A novel mutation and review. International Journal of Pediatric Otorhinolaryngology. pp. 1610-1615. ISSN 0165-5876