Items where Author is "Jalilian, N."

Article

(2020) Upregulation ofMTOR,RPS6KB1, andEIF4EBP1in the whole blood samples of Iranian patients with multiple sclerosis compared to healthy controls. Metabolic Brain Disease. pp. 1309-1316. ISSN 0885-7490

(2017) A Novel Pathogenic Variant in the MITF Gene Segregating with a Unique Spectrum of Ocular Findings in an Extended Iranian Waardenburg Syndrome Kindred. Molecular Syndromology. pp. 195-200. ISSN 1661-8769

(2017) SOX10 mutation causes Waardenburg syndrome associated with distinctive phenotypic features in an Iranian family: A clue for phenotype-directed genetic analysis. International Journal of Pediatric Otorhinolaryngology. pp. 122-126. ISSN 0165-5876

(2016) Does PTEN gene mutation play any role in Li-Fraumeni syndrome. Medical journal of the Islamic Republic of Iran. p. 378. ISSN 1016-1430 (Print) 1016-1430 (Linking)

(2015) Molecular and clinical characterization of Waardenburg syndrome type I in an Iranian cohort with two novel PAX3 mutations. Gene. pp. 302-307. ISSN 0378-1119

(2015) A novel mutation in the PAX3 gene causes Waardenburg syndrome type I in an Iranian family. International Journal of Pediatric Otorhinolaryngology. pp. 1736-1740. ISSN 0165-5876