Repository of Research and Investigative Information
Shahid Sadoughi University of Medical Sciences
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(2022) Mitochondrial Mutations in Protein Coding Genes of Respiratory Chain Including Complexes Iv, V, And Mt-Trna Genes Are Associated Risk Factors for Congenital Heart Disease. EXCLI Journal. pp. 1306-1330.
(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 NKX2.1 gene in a cohort of Iranian pediatric patients with congenital hypothyroidism (CH). Physiology International. pp. 261-277.
(2022) Novel Point Mutations in 3'-Untranslated Region of GATA4 Gene Are Associated with Sporadic Non-syndromic Atrial and Ventricular Septal Defects. Current Medical Science. pp. 129-143.
(2022) Novel Point Mutations in 3�-Untranslated Region of GATA4 Gene Are Associated with Sporadic Non-syndromic Atrial and Ventricular Septal Defects. Current Medical Science. pp. 129-143.
(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) Polymorphisms of sperm protamine genes and CMA3 staining in infertile men with varicocele Polimorfismos de los genes de la protamina espermática y tinción CMA3 en varones infértiles con varicocele. Revista Internacional de Andrologia. pp. 7-13.