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| Issue |
Title |
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| Vol 29, No 5 (2025) |
A family case of a rare Xq28 duplication |
Abstract
PDF (Eng)
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A. E. Kopytova, E. N. Tolmacheva, D. A. Emelina, O. S. Glotov, V. V. Miroshnikova, T. S. Usenko, O. Yu. Vasilyeva, E. D. Kasyanov, E. A. Fonova, I. V. Makarov, A. D. Lobanov, G. E. Mazo, S. N. Pchelina, I. N. Lebedev |
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| Vol 29, No 5 (2025) |
A familial case of interstitial deletion of the short arm of chromosome 6p22.3-p24.3 in twins with severe delay in psychomotor and speech development |
Abstract
PDF (Eng)
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G. D. Moskvitin, D. B. Kochkina, E. E. Gurinova, D. A. Fedotov, L. V. Bekenieva, A. A. Kashevarova, A. L. Sukhomyasova, I. N. Lebedev, N. R. Maximova |
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| Vol 29, No 5 (2025) |
Study of the meiotic segregation of chromosome 7 with a paracentric inversion in spermatosoa of a heterozygous |
Abstract
PDF (Eng)
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M. M. Antonova, D. A. Yurchenko, Zh. G. Markova, N. V. Shilova |
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| Vol 29, No 5 (2025) |
Familial translocation between chromosomes 3 and 10: meiotic segregation, diagnostics and clinical features of chromosomal |
Abstract
PDF (Eng)
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A. V. Vozilova, A. S. Tarasova, E. A. Ivanov, V. P. Pushkarev, N. I. Nalyotova, A. I. Pobedinskaya, A. S. Sabitova, N. V. Shilova |
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| Vol 29, No 5 (2025) |
Molecular genetic study of triploidy and the hydatidiform mole in pregnancy loss: analysis of 10,000 consecutive cases |
Abstract
PDF (Eng)
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V. P. Pushkarev, A. S. Masycheva, E. A. Glazyrina, T. E. Serebrenikova, V. B. Chernykh |
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| Vol 29, No 5 (2025) |
A rare case of uniparental disomy 9 concomitant with low-level mosaicism |
Abstract
PDF (Eng)
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A. S. Iakovleva, Zh. G. Markova, L. A. Bessonova, N. V. Shilova |
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