APPLICATION OF METHOD FISH (FLUORESCENCE $IN~SITU$ HYBRIDIZATION) IN PRENATAL AND POSTNATAL DIAGNOSTICS OF CHROMOSOMAL ANOMALIES

Authors

  • M. S. Manvelyan Chair of Cytology and Genetics, YSU, Armenia

DOI:

https://doi.org/10.46991/PYSU:B/2004.38.2.103

Keywords:

molecular-cytogenetic method, fluorescence $in~situ$ hybridization, chromosomal pathology, chromosomal anomalies

Abstract

For the first time the molecular-cytogenetic method of fluorescence in situ hybridization (FISH) was widely used in Armenia in prenatal and postnatal diagnostics of 30 patients with different forms of chromosomal pathology. Application of FISH method in cytogenetic practice of Armenia increased the efficiency of diagnostics of chromosomal anomalies.

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Published

2004-04-30

How to Cite

Manvelyan, M. S. 2004. “APPLICATION OF METHOD FISH (FLUORESCENCE $IN~SITU$ HYBRIDIZATION) IN PRENATAL AND POSTNATAL DIAGNOSTICS OF CHROMOSOMAL ANOMALIES”. Proceedings of the YSU B: Chemical and Biological Sciences 38 (2 (204):103-8. https://doi.org/10.46991/PYSU:B/2004.38.2.103.

Issue

Vol. 38 No. 2 (204) (2004)

Section

Biology

License

Copyright (c) 2004 Proceedings of the YSU

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This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.