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Gholipoorfeshkecheh, R. and Swati Agarwala and Santhosh, K. and Savitha, M. R. and Narayanappa, D. and Ramachandra, N. B. (2020) Nuclear Co-repressor 1: A Potential Candidate Gene in the Manifestation of Congenital Heart Diseases. International Journal of Human Genetics, 20 (2). pp. 55-65. ISSN 2456-6330
Gholipoorfeshkecheh, R. and Agarwala, S. and Krishnappa, S. and Savitha, M. R. and Narayanappa, D. and Ramachandra, N. B. (2020) Variants in HEY genes manifest in ventricular septal defects of congenital heart disease. Gene Reports, 19.
Dinesh, S. M. and Lingaiah, K. and Savitha, M. R. and Krishnamurthy, B. and Narayanappa, D. and Ramachandra, N. B. (2011) GATA4 specific nonsynonymous single-nucleotide polymorphisms in congenital heart disease patients of Mysore, India. GENETIC TESTING AND MOLECULAR BIOMARKERS, 15 (10). pp. 715-720.
Kusuma, L. and Dinesh, S. M. and Savitha, M. R. and Krishnamurthy, B. and Narayanappa, D. and Ramachandra, N. B. (2011) A maiden report on CRELD1 single-nucleotide polymorphism association in congenital heart disease patients of Mysore, South India. GENETIC TESTING AND MOLECULAR BIOMARKERS, 15 (7-8). pp. 483-487.
Dinesh, S. M. and Kusuma, L. and Smitha, R. and Savitha, M. R. and Krishnamurthy, B. and Narayanappa, D. and Ramachandra, N. B. (2010) Single-Nucleotide Polymorphisms of NKX2.5 Found in Congenital Heart Disease Patients of Mysore, South India. Genetic Testing and Molecular Biomarkers, 14 (6). pp. 873-879. ISSN 1945-0257
