(2012) A Girl with 45,X/46,XX Turner Syndrome and Salt Wasting Form of Congenital Adrenal Hyperplasia Due to Regulatory Changes. Clinical Laboratory. pp. 1063-1066. ISSN 1433-6510

(2012) Mutation Analysis of the CYP21A2 Gene in the Iranian Population. Genetic Testing and Molecular Biomarkers. pp. 82-90. ISSN 1945-0265

(2012) Screening of OTOF mutations in Iran: A novel mutation and review. International Journal of Pediatric Otorhinolaryngology. pp. 1610-1615. ISSN 0165-5876

(2011) Impact of Consanguineous Marriages in GJB2-Related Hearing Loss in the Iranian Population: A Report of a Novel Variant. Genetic Testing and Molecular Biomarkers. pp. 489-493. ISSN 1945-0265

(2011) Molecular Diagnosis of Congenital Adrenal Hyperplasia in Iran: Focusing on CYP21A2 Gene. Iranian Journal of Pediatrics. pp. 139-150. ISSN 2008-2142