Creation and Application of Test-Kits for Hereditary Diseases Gene Diagnostics to Medical Practice

Authors

  • L. A. Livshits Institute of Molecular Biology and Genetics, NAS of Ukraine, Kyiv
  • V. M. Pampukha Institute of Molecular Biology and Genetics, NAS of Ukraine, Kyiv
  • O. A. Yasinska Institute of Molecular Biology and Genetics, NAS of Ukraine, Kyiv
  • G. B. Livshits Institute of Molecular Biology and Genetics, NAS of Ukraine, Kyiv
  • N. V. Hryshchenko Institute of Molecular Biology and Genetics, NAS of Ukraine, Kyiv
  • S. A. Kravchenko nstitute of Molecular Biology and Genetics, NAS of Ukraine, Kyiv
  • M. V. Nechyporenko Institute of Molecular Biology and Genetics, NAS of Ukraine, Kyiv
  • G. V. Yelska Institute of Molecular Biology and Genetics, NAS of Ukraine, Kyiv

DOI:

https://doi.org/10.15407/scin1.03.062

Keywords:

mutations, cystic fibrosis, hereditary chromatosis, Martin-Bell syndrome (fragile X), azoospermia factor, DNA-diagnosis, PCR.

Abstract

Test-systems and their exhibition working samples based on the DNA-analysis for diagnosis most spread in Ukraine monogenic hereditary disorders such as: cystic fibrosis, hereditary chromatosis, Martin-Bell syndrome (fragile X), genetic forms of male infertility were elaborated. The elaborated test-systems would be used in special medical centers for medical genetics, pediatric and in IVF clinics, which apply assessment reproductive technologies

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Published

2024-05-21