DIFFERNTIAL DIAGNOSIS OF DELETION AND UNIPARENTAL DISOMY IN 15Q11.2-Q13 LOCUS


  • S. Yu. Chernushyn Institute of Molecular Biology and Genetics, National Academy of Sciences of Ukraine
  • S.A. Kravchenko Institute of Molecular Biology and Genetics, National Academy of Sciences of Ukraine
  • N.V. Hryshchenko Institute of Molecular Biology and Genetics, National Academy of Sciences of Ukraine
Keywords: Prader-Willi; Angelman; Deletions; Uniparentaldisomy

Abstract

DIFFERNTIAL DIAGNOSIS OF DELETION AND UNIPARENTAL DISOMY IN 15Q11.2-Q13 LOCUS

References

1. S. C. Ramsden, J. Clayton-Smith, R. Birch, and K. Buiting, “Practice guidelines for the molecular analysis of Prader-Willi and Angelman syndromes,” BMC Medical Genetics, vol. 11, no. 1, May 2010.

2. L. Kalsner and S. J. Chamberlain, “Prader-Willi, Angelman, and 15q11-q13 Duplication Syndromes,” Pediatric Clinics of North America, vol. 62, no. 3, pp. 587–606, Jun. 2015.

3. Robinson, W. P, “Mechanisms leading to uniparentaldisomy and their clinical consequences” BioEssays, vol. 22, no. 5, pp. 452–459, 2000.
Published
2019-11-07
How to Cite
Chernushyn, S. Y., Kravchenko, S., & Hryshchenko, N. (2019). DIFFERNTIAL DIAGNOSIS OF DELETION AND UNIPARENTAL DISOMY IN 15Q11.2-Q13 LOCUS. Biological Markers in Fundamental and Clinical Medicine (scientific Journal), 3(1), 30-31. https://doi.org/10.29256/v.03.01.2019.escbm17
Section
Selected abstracts