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(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) In silico structural, functional and pathogenicity evaluation of a novel mutation: An overview of HSD3B2 gene mutations. Gene. pp. 215-221. ISSN 0378-1119
(2012) Mutation Analysis of the CYP21A2 Gene in the Iranian Population. Genetic Testing and Molecular Biomarkers. pp. 82-90. 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