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Статьи, опубликованные только в Russian J. of Genetics, № 11 – 2021 г.

Novel Mutations in LRTOMT Associated with Congenital Profound Sensorineural Hearing Loss in a Chinese Patient
Y. Wang, Y. Ma, Y. Qin, Zh. Zeng, Zh. Zhong, Y. Qi, Y. Liu
     Pages 1322-1327


The Correlation of MTHFR SNPs, Homocysteine, and Conventional Risk Predictors with Coronary Aartery Disease
R. Masud, A.U.H. Khan, H.Z. Baqai, А. Iqbal
     Pages 1328-1336