Generation of iPS cell line (ICGi040-A) from skin fibroblasts of a patient with ring small supernumerary marker chromosome 4 von Gridina, M.M., Nurislamov, A.R., Minina, J.M., Lopatkina, M.E., Drozdov, G.V., Vasilyev, S.A., Minaycheva, L.I., Belyaeva, E.O., Nikitina, T.V., Kashevarova, A.A., Lebedev, I.N., Karamysheva, T.V., Rubtsov, N.B., Serov, O.L.

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Generation of iPSC line ICGi024-A from human skin fibroblasts of a patient with ring chromosome 18 von Khabarova, A.A., Pristyazhnyuk, I.E., Orlova, P.A., Nikitina, T.V., Kashevarova, A.A., Lopatkina, M.E., Belyaeva, E.O., Sukhanova, N.N., Nazarenko, L.P., Lebedev, I.N., Serov, O.L.

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Generation of an induced pluripotent stem cell line ICGi030-A from a Wilson's disease patient carrying a frameshift mutation p.Lys1013fs and missense mutation p.H1069Q in the ATP7B... von Zhigalina, D.I., Malakhova, A.A., Vasilyeva, O.Yu, Grigor'eva, E.V., Sivtsev, A.A., Kolesnikov, N.A., Lopatkina, M.E., Savchenko, R.R., Zhalsanova, I.Zh, Postrigan', A.E., Zarubin, A.A., Nikitina, T.V., Bueverov, A.O., Bogomolov, P.O., Zakian, S.M., Skryabin, N.A.

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Establishment of an induced pluripotent stem cell line (ICGi025-A) from fibroblasts of a patient with 46,XY,r(8)/45,XY,–8 mosaicism von Gridina, M.M., Nikitina, T.V., Orlova, P.A., Minina, J.M., Kashevarova, A.A., Yakovleva, Yu.S., Lopatkina, M.E., Vasilyev, S.A., Fedotov, D.A., Mikhailik, L.I., Nazarenko, L.P., Lebedev, I.N., Serov, O.L.

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Induced pluripotent stem cell line, IMGTi003-A, derived from skin fibroblasts of an intellectually disabled patient with ring chromosome 13 von Nikitina, T.V., Menzorov, A.G., Kashevarova, A.A., Gridina, M.M., Khabarova, A.A., Yakovleva, Yu.S., Lopatkina, M.E., Pristyazhnyuk, I.E., Vasilyev, S.A., Serov, O.L., Lebedev, I.N.

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Generation of the induced pluripotent stem cell line, ICAGi002-A, from unaffected carrier megabase scaled duplication involving the CNTN6 gene von Gridina, M.M., Nikitina, T.V., Pristyazhnyuk, I.E., Kashevarova, A.A., Lopatkina, M.E., Vasilyev, S.A., Nazarenko, L.P., Lebedev, I.N., Serov, O.L.

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Generation of four iPSC lines from two siblings with a microdeletion at the CNTN6 gene and intellectual disability von Shnaider, T.A., Pristyazhnyuk, I.E., Menzorov, A.G., Matveeva, N.M., Nikitina, T.V., Khabarova, A.A., Skryabin, N.A., Kashevarova, A.A., Lopatkina, M.E., Nazarenko, L.P., Lebedev, I.N., Serov, O.L.

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Generation of two iPSC lines (IMGTi001-A and IMGTi001-B) from human skin fibroblasts with ring chromosome 22 von Nikitina, T.V., Menzorov, A.G., Kashevarova, A.A., Gridina, M.M., Khabarova, A.A., Yakovleva, Yu.S., Lopatkina, M.E., Kizilova, E.A., Vasilyev, S.A., Serov, O.L., Lebedev, I.N.

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Supplementary Material for: Skewed X-Chromosome Inactivation as a Possible Marker of X-Linked CNV in Women with Pregnancy Loss von E.A., Fonova, E.N., Tolmacheva, A.A., Kashevarova, E.A., Sazhenova, T.V., Nikitina, M.E., Lopatkina, O.Y., Vasilyeva, A.A., Zarubin, T.N., Aleksandrova, S.Y., Yuriev, N.A., Skryabin, V.A., Stepanov, I.N., Lebedev

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Supplementary Material for: Differential DNA Methylation of the IMMP2L Gene in Families with Maternally Inherited 7q31.1 Microdeletions is Associated with Intellectual Disability a... von Vasilyev, S.A., Skryabin, N.A., Kashevarova, A.A., Tolmacheva, E.N., Savchenko, R.R., Vasilyeva, O.Y., Lopatkina, M.E., Zarubin, A.A., Fishman, V.S., Belyaeva, E.O., Filippova, M.O., Shorina, A.R., Maslennikov, A.B., Shestovskikh, O.L., Gayner, T.A., Čulić, V., Vulić, R., Nazarenko, L.P., Lebedev, I.N.

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