Study of SNRPN genetic and epigenetic mutations in Prader-Willi and Angelman patients von Chernushyn, S.Yu., Hryshchenko, N.V.

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Development of MLPA approach for SNP detection in MTHFR, F5 and F2 genes von Kravchenko, S.A., Chernushyn, S.Yu., Kucherenko, A.M., Soloviov, O.O., Livshits, L.A.

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Human genome mutation and rearrangement studies – the way to investigate monogenic and complex disease pathogenesis von Livshits, L.A., Kravchenko, S.A., Nechyporenko, M.V., Pampukha, V.M., Hryshchenko, N.V., Livshyts, G.B., Soloviov, O.O., Tatarskyy, P.F., Fesai, O.A., Chernushyn, S.Yu., Kucherenko, A.M., Gulkovskyy, R.V.

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