Repository of Research and Investigative Information

Repository of Research and Investigative Information

Ilam University of Medical Sciences

Items where Author is "Rabbani, B."

Tue Aug 16 10:41:48 2022
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: 10.

Article

(2014) The promise of whole-exome sequencing in medical genetics. Journal of Human Genetics. pp. 5-15. ISSN 1434-5161

(2013) An Overview of Mutation Detection Methods in Genetic Disorders. Iranian Journal of Pediatrics. pp. 375-388. ISSN 2008-2142

(2012) 21-Hydroxylase Deficiency: Newborn Screening in Iran? Iranian Journal of Pediatrics. pp. 279-280. ISSN 2008-2142

(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

(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

(2009) Statistical study of 35delG mutation of GJB2 gene: A meta-analysis of carrier frequency. International Journal of Audiology. pp. 363-370. ISSN 1499-2027

This list was generated on Tue Aug 16 10:41:48 2022 +0430.