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Сomparative genomic hybridization in prenatal diagnosis
https://doi.org/10.25557/2073-7998.2020.03.60-61
Abstract
Molecular karyotyping in our study showed a 6.4% increase in the detectability of chromosomal aberrations compared to classical cytogenetic methods, but their combined application is necessary to determine and/or clarify the nature of microscopic or submicroscopic anomalies and to identify balanced rearrangements.
About the Authors
V. A. Gnetetskaya
Medical Genetics center, Group of companies «Mother and child»
Russian Federation
J. A. Tarasova
Medical Genetics center, Group of companies «Mother and child»
Russian Federation
E. S. Kuznetsova
Medical Genetics center, Group of companies «Mother and child»
Russian Federation
M. A. Ermakova
Medical Genetics center, Group of companies «Mother and child»
Russian Federation
V. L. Izhevskaya
Research Centre for Medical Genetics
Russian Federation
For citations:
Gnetetskaya V.A.,
Tarasova J.A.,
Kuznetsova E.S.,
Ermakova M.A.,
Izhevskaya V.L.
Сomparative genomic hybridization in prenatal diagnosis. Medical Genetics. 2020;19(3):60-61.
(In Russ.)
https://doi.org/10.25557/2073-7998.2020.03.60-61
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