Items where Author is "Krishnappa, S."

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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.

Gholipoorfeshkecheh, R. and Agarwala, S. and Kavya, G. and Krishnappa, S. and Savitha, M. R. and Ramachandra, N. B. (2020) Whole-exome sequencing and homozygosity mapping identify variants in NCOR1 and MAP2K3 associated with non-syndromic congenital heart defects. Egyptian Journal of Medical Human Genetics, 21 (1).

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