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    A family case of a rare Xq28 duplication Autor Kopytova, A E, Tolmacheva, E N, Emelina, D A, Glotov, O S, Miroshnikova, V V, Usenko, T S, Vasilyeva, O Yu, Makarov, I V, Lobanov, A D, Mazo, G E, Pchelina, S N, Lebedev, I N

    ISSN: 2500-0462
    Vydáno: 01.09.2025
    “…Genetic factors contribute to the etiology of intellectual disability in 25-50 % of cases. Chromosomal abnormalities, such as microdeletions and…”
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    Journal Article
  2. 2

    A family case of a rare Xq28 duplication Autor Kopytova, A. E., Tolmacheva, E. N., Emelina, D. A., Glotov, O. S., Miroshnikova, V. V., Usenko, T. S., Vasilyeva, O. Yu, Kasyanov, E. D., Fonova, E. A., Makarov, I. V., Lobanov, A. D., Mazo, G. E., Pchelina, S. N., Lebedev, I. N.

    ISSN: 2500-3259, 2500-0462, 2500-3259
    Vydáno: Russia (Federation) Siberian Branch of the Russian Academy of Sciences, Federal Research Center Institute of Cytology and Genetics, The Vavilov Society of Geneticists and Breeders 01.09.2025
    “…   Genetic factors contribute to the etiology of intellectual disability in 25–50 % of cases. Chromosomal abnormalities, such as microdeletions and…”
    Získat plný text
    Journal Article