Kalayinia, S., Ghasemi, S., & Mahdieh, N. (2019). A comprehensive in silico analysis, distribution and frequency of human Nkx2-5 mutations; A critical gene in congenital heart disease. J Cardiovasc Thorac Res.
Styl ChicagoKalayinia, Samira, Serwa Ghasemi, a Nejat Mahdieh. "A Comprehensive in Silico Analysis, Distribution and Frequency of Human Nkx2-5 Mutations; A Critical Gene in Congenital Heart Disease." J Cardiovasc Thorac Res 2019.
Citace podle MLAKalayinia, Samira, Serwa Ghasemi, a Nejat Mahdieh. "A Comprehensive in Silico Analysis, Distribution and Frequency of Human Nkx2-5 Mutations; A Critical Gene in Congenital Heart Disease." J Cardiovasc Thorac Res 2019.
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