Trisomy 21 Mosaicism: We May All Have a Touch of Down Syndrome von Hultén, M.A., Jonasson, J., Iwarsson, E., Uppal, P., Vorsanova, S.G., Yurov, Y.B., Iourov, I.Y.

Volltext

Somatic Genome Variations in Health and Disease von Iourov, I Y, Vorsanova, S G, Yurov, Y B

Volltext

Somatic Cell Genomics of Brain Disorders: A New Opportunity to Clarify Genetic-Environmental Interactions von Iourov, I.Y., Vorsanova, S.G., Yurov, Y.B.

Volltext

Classification and monomer-by-monomer annotation dataset of suprachromosomal family 1 alpha satellite higher-order repeats in hg38 human genome assembly von Uralsky, L.I., Shepelev, V.A., Alexandrov, A.A., Yurov, Y.B., Rogaev, E.I., Alexandrov, I.A.

Volltext

Causes and Consequences of Genome Instability in Psychiatric and Neurodegenerative Diseases von Iourov, I. Y., Vorsanova, S. G., Kurinnaia, O. S., Zelenova, M. A., Vasin, K. S., Yurov, Y. B.

Volltext

Visualization of interphase chromosomes in postmitotic cells of the human brain by multicolour banding (MCB) von Iourov, I Y, Liehr, T, Vorsanova, S G, Kolotii, A D, Yurov, Y B

Volltext

Unexplained autism is frequently associated with low-level mosaic aneuploidy von Yurov, Y B, Vorsanova, S G, Iourov, I Y, Demidova, I A, Beresheva, A K, Kravetz, V S, Monakhov, V V, Kolotii, A D, Voinova-Ulas, V Y, Gorbachevskaya, N L

Volltext

Molecular Cytogenetics and Cytogenomics of Brain Diseases von Iourov, I Y, Vorsanova, S G, Yurov, Y B

Volltext

Ontogenetic Variation of the Human Genome von Yurov, Y B, Vorsanova, S G, Iourov, I Y

Volltext

Serologic Markers of Autism Spectrum Disorder von Khramova, T. V., Kaysheva, Anna L., Ivanov, Y. D., Pleshakova, T. O., Iourov, I. Y., Vorsanova, S. G., Yurov, Y. B., Schetkin, A. A., Archakov, A. I.

Volltext

Molecular Cytogenetic Diagnosis and Somatic Genome Variations von Vorsanova, S G, Yurov, Y B, Soloviev, I V, Iourov, I Y

Volltext

Annotation of suprachromosomal families reveals uncommon types of alpha satellite organization in pericentromeric regions of hg38 human genome assembly von Shepelev, V.A., Uralsky, L.I., Alexandrov, A.A., Yurov, Y.B., Rogaev, E.I., Alexandrov, I.A.

Volltext

Combination of atomic force microscopy and mass spectrometry for the detection of target protein in the serum samples of children with autism spectrum disorders von Kaysheva, A L, Pleshakova, T O, Kopylov, A T, Shumov, I D, Iourov, I Y, Vorsanova, S G, Yurov, Y B, Ziborov, V S, Archakov, A I, Ivanov, Y D

Volltext

Intercellular Genomic (Chromosomal) Variations Resulting in Somatic Mosaicism: Mechanisms and Consequences von Iourov, I., Vorsanova, S., Yurov, Y.

Volltext

Dynamic mosaicism manifesting as loss, gain and rearrangement of an isodicentric Y chromosome in a male child with growth retardation and abnormal external genitalia von Iourov, I.Y., Vorsanova, S.G., Liehr, T., Monakhov, V.V., Soloviev, I.V., Yurov, Y.B.

Volltext

Multicolor fluorescent in situ hybridization on post-mortem brain in schizophrenia as an approach for identification of low-level chromosomal aneuploidy in neuropsychiatric disease... von Yurov, Yuri B, Vostrikov, Viktor M, Vorsanova, Svetlana G, Monakhov, Victor V, Iourov, Ivan Y

Volltext

Definition of a new alpha satellite suprachromosomal family characterized by monomeric organization von AIexandrov, I.A., Medvedev, L.I., Mashkova, T.D., Kisselev, L.L., Romanova, L.Y., Yurov, Y.B.

Volltext

The phylogeny of human chromosome specific alpha satellites von ALEXANDROV, I. A, MITKEVICH, S. P, YUROV, Y. B

Volltext

High resolution multicolor fluorescence in situ hybridization using cyanine and fluorescein dyes : rapid chromosome identification by directly fluorescently labeled alphoid DNA pro... von YUROV, YU. B, SOLOVIEV, I. V, VORSANOVA, S. G, MARCAIS, B, ROIZES, G, LEWIS, R

Volltext

Efficient identification of marker chromosomes in 27 patients by stepwise hybridization with alpha-satellite DNA probes von PLATTNER, R, HEEREMA, N. A, YUROV, Y. B, PALMER, C. G

Volltext