Search Results - Min’zhenkova, M. E

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  1. 1
    Geneticl and clinical characteristics of 22q11.2 deletion syndrome

    Geneticl and clinical characteristics of 22q11.2 deletion syndrome by Kozlova, Yu. O, Zabnenkova, V. V, Shilova, N. V, Min’zhenkova, M. E, Antonenko, V. G, Kotlukova, N. P, Simonova, L. V, Kazantseva, I. A, Levchenko, E. G, Bombardirova, T. D, Zolotukhina, T. V, Polyakov, A. V

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  2. 2
    Influence of human peripheral blood samples preprocessing on the quality of Hi-C libraries

    Influence of human peripheral blood samples preprocessing on the quality of Hi-C libraries by Gridina, M M, Vesna, E, Minzhenkova, M E, Shilova, N V, Ryzhkova, O P, Nazarenko, L P, Belyaeva, E O, Lebedev, I N, Fishman, V S

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  3. 3
    Molecular cytogenetic characteristics of small supernumerary marker chromosomes 15 and 22 in asymptomatic carriers

    Molecular cytogenetic characteristics of small supernumerary marker chromosomes 15 and 22 in asymptomatic carriers by Yurchenko, DA, Markova, ZhG, Minzhenkova, ME, Vorontsova, EO, Shilova, NV

    Published in Bulletin of RSMU
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  4. 4
    Induced pluripotent stem cell line, ICAGi001-A, derived from human skin fibroblasts of a patient with 2p25.3 deletion and 2p25.3-p23.3 inverted duplication

    Induced pluripotent stem cell line, ICAGi001-A, derived from human skin fibroblasts of a patient with 2p25.3 deletion and 2p25.3-p23.3 inverted duplication by Khabarova, A.A., Pristyazhnyuk, I.E., Nikitina, T.V., Gayner, T.A., Torkhova, N.B., Skryabin, N.A., Kashevarova, A.A., Babushkina, N.P., Markova, Zh.G., Minzhenkova, M.E., Nazarenko, L.P., Shilova, N.V., Shorina, A.R., Lebedev, I.N., Serov, O.L.

    Published in Stem cell research
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  5. 5
    Characterization of a complex chromosomal rearrangement in a girl with PURA syndrome

    Characterization of a complex chromosomal rearrangement in a girl with PURA syndrome by Minzhenkova, ME, Yurchenko, DA, Semenova, NA, Markova, ZG, Tarlycheva, AA, Shilova, NV

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  6. 6
    Generation and application of dynamic standard reference intervals for analyzing results of comparative genomic hybridization

    Generation and application of dynamic standard reference intervals for analyzing results of comparative genomic hybridization by Min’zhenkova, M. E., Shilova, N. V., Markova, Zh. G., Antonenko, V. G., Lebedev, I. N., Kozlova, Yu. O., Zemlyakova, V. V., Zolotukhina, T. V.

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  7. 7
    Evaluation of Risk Factors for the Birth of Children with Chromosomal Imbalance in Carriers of Autosomal Reciprocal Translocations

    Evaluation of Risk Factors for the Birth of Children with Chromosomal Imbalance in Carriers of Autosomal Reciprocal Translocations by Shilova, N. V., Minzhenkova, M. E., Antonenko, V. G.

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  8. 8
    Complex Chromosomal Rearrangement Involving Chromosomes 10 and 11, Accompanied by Two Adjacent 11p14.1p13 and 11p13p12 Deletions, Identified in a Patient with WAGR Syndrome

    Complex Chromosomal Rearrangement Involving Chromosomes 10 and 11, Accompanied by Two Adjacent 11p14.1p13 and 11p13p12 Deletions, Identified in a Patient with WAGR Syndrome by Marakhonov, Andrey V, Vasilyeva, Tatyana A, Minzhenkova, Marina E, Sukhanova, Natella V, Sparber, Peter A, Andreeva, Natalya A, Teleshova, Margarita V, Baybagisova, Fatima K-M, Shilova, Nadezhda V, Kutsev, Sergey I, Zinchenko, Rena A

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