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(2022) Mutational Analysis of the <i>VPREB1</i> Gene of Pre-BCR Complex in a Cohort of Sporadic Pediatric Patients With B-Cell Acute Lymphoblastic Leukemia. Journal of Pediatric Hematology Oncology. pp. 210-219. ISSN 1077-4114
(2022) Mutational Analysis of the VPREB1 Gene of Pre-BCR Complex in a Cohort of Sporadic Pediatric Patients with B-Cell Acute Lymphoblastic Leukemia. Journal of Pediatric Hematology/Oncology. pp. 210-219.
(2022) Mutational and bioinformatics analysis of the <i>NKX2</i>.1 gene in a cohort of Iranian pediatric patients with congenital hypothyroidism (CH). Physiology International. pp. 261-277. ISSN 2498-602X
(2022) Mutational and bioinformatics analysis of the NKX2.1 gene in a cohort of Iranian pediatric patients with congenital hypothyroidism (CH). Physiology International. pp. 261-277.
(2021) In-silico study to identify the pathogenic single nucleotide polymorphisms in the coding region of CDKN2A gene. Iranian Journal of Pediatric Hematology and Oncology. pp. 114-133.
(2020) MicroRNAs as a New Molecular Biomarker for Diagnosis and Prognosis of T-cell Acute Lymphoblastic Leukemia (T-ALL): A Systematic Review. Iranian Journal of Pediatric Hematology and Oncology. pp. 184-199. ISSN 2008-8892