Analysis of 17p11.2 chromosome region rearrangements in CMT1 patients from Ukraine von Hryshchenko, N.V., Livshits, L.A.

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Association of the leukemia inhibitory factor gene polymorphism rs929271 with idiopathic mild intellectual disability von Gulkovskyi, R.V., Volkova, L.S., Livshits, L.A.

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Polymorphic short tandem repeats for PCR-based diagnosis of the Charcot-Marie-Tooth 1A duplication in Ukraine von Hryshchenko, N.V., Kravchenko, S.A., Livshits, L.A.

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Novel gene PUS3 c.A212G mutation in Ukrainian family with intellectual disability von Gulkovskyi, R.V., Chernushyn, S.Y., Livshits, L.A.

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Association of the EPHA1 gene polymorphism with idiopathic mild intellectual disability von Gulkovskyi, R.V., Livshits, L.A., Sivolob, A.V.

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Development of ARMS PCR tests for detection of common CFTR gene mutations von Soloviov, O.O., Pampukha, V.M., Livshits, L.A.

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Study on the IFNL4 gene ss469415590 variant in Ukrainian population von Kucherenko, A.M., Pampukha, V.M., Livshits, L.A.

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Implementation of the quantitative Real-Time PCR for the molecular-genetic diagnostics of spinal muscular atrophy von Soloviov, O.O., Livshits, G.B., Podlesnaya, S.S., Livshits, L.A.

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Distribution of FSHR307 and FSHR680 allelic variants of FSH receptor gene exon 10 in females from Ukraine von Livshyts, G.B., Podlesnaja, S.S., Kravchenko, S.A., Livshits, L.A.

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Study on occurrence of the IVS8-5T allele of the CFTR gene in Ukrainian males with spermatogenesis failure von Fesai, O.A., Kravchenko, S.A., Zinchenko, V.M., Livshits, L.A.

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IFN-l-3 (IL28B) genotyping by restriction fragment length polymorphism method: detection polymorphism of rs12979860 von Pampukha, V.M., Kravchenko, S.A., Moroz, L.V., Livshits, L.A.

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EPHA1 gene SNPs analysis in population of Ukraine von Gulkovskyi, R.V., Chernushyn, S.Y., Kravchenko, S.A., Bychkova, G.M., Livshits, L.A.

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Association of IL8 and IL10 gene allelic variants with ischemic stroke risk and prognosis von Kucherenko, A.M., Shulzhenko, D.V., Kuznetsova, S.M., Demydov, S.V., Livshits, L.A.

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Ischemic stroke in Ukrainian population: possible involvement of the F2 G20210A, F5 G1691A and MTHFR C677T gene variants von Tatarskyy, P.F., Kucherenko, A.M., Kravchenko, S.A., Shulzhenko, D.V., Kuznetsova, S.M., Livshits, L.A.

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Study on possible role of CYP1A1, GSTT1, GSTM1, GSTP1, NAT2 and ADRB2 genes polymorphisms in bronchial asthma development in children von Tatarskyy, P.F., Chumachenko, N.G., Kucherenko, A.M., Gulkovskyi, R.V., Arabskaya, L.P., Smirnova, O.A., Tolkach, S.I., Antipkin, Yu.G., Livshits, L.A.

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