Repository of Research and Investigative Information

Repository of Research and Investigative Information

Ilam University of Medical Sciences

Items where Author is "Ashtiani, M. T. H."

Fri Apr 19 11:10:48 2024
Up a level
Export as [feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Group by: Item Type | No Grouping
Jump to: Article
Number of items: 4.

Article

(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

This list was generated on Thu Apr 18 16:09:03 2024 +0330.