Перегляд за автором "Vorsanova, S.G."

Результати 1-4 з 4

Chimerism and multiple numerical chromosome imbalances in a spontaneously aborted fetus

Vorsanova, S.G.; Iourov, I.Y.; Demidova, I.A.; Kirillova, E.A.; Soloviev, I.V.; Yurov, Y.B. (Цитология и генетика, 2006)

We report on a case of chimerism and multiple abnormalities of chromosomes 21, X and Y in spontaneous abortion specimen. To the best our knowledge the present case is the first documented chimera in a spontaneously aborted ...
Fluorescence intensity profiles of in situ hybridization signals depict genome architecture within human interphase nuclei

Iourov, I.Y.; Vorsanova, S.G.; Yurov, Y.B. (2008)

An approach towards construction of two-dimensional (2D) and three-dimensional (3D) profiles of interphase chromatin architecture by quantification of fluorescence in situ hybridization (FISH) signal intensity is proposed. ...
Non-disjunction of chromosome 21, alphoid DNA variation, and sociogenetic features of Down syndrome

Vorsanova, S.G.; Iourov, I.Y.; Beresheva, A.K.; Demidova, I.A.; Monakhov, V.V.; Kravets, V.S.; Bartseva, O.B.; Goyko, E.A.; Soloviev, I.V.; Yurov, Y.B. (Цитология и генетика, 2005)

The analysis of non-disjunction of chromosome 21 and alphoid DNA variation by using cytogenetic and molecular cytogenetic techniques (quantitative fluorescence in situ hybridization) in 74 nuclear families was performed. ...
Pericentric inversion inv(7)(p11q21.1): report on two cases and genotype-phenotype correlations

Vorsanova, S.G.; Iourov, I.Y.; Demidova, I.A.; Kolotii, A.D.; Soloviev, I.V.; Yurov, Y.B. (Цитология и генетика, 2006)

We report on two unrelated cases of pericentric inversion 46,XY,inv(7)(p11q21.1) associated with distinct pattern of malformation including mental retardation, development delay, ectrodactyly, facial dismorphism, high ...

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Перегляд за автором "Vorsanova, S.G."

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Перегляд за автором "Vorsanova, S.G."

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