RNDr. Iveta Valášková, Ph.D.
Assistant professor, Institute of Medical Genetics and Genomics
| Phone: | +420 532 23 4718 |
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| E‑mail: |
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Publications
Total number of publications: 73
2019
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Mutation R591C associated with long QT syndrome type 1: clinical, genetic, and functional analysis
Year: 2019, type: Conference abstract
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Novorozenecký screening cystické fibrózy a diagnostika CFSPID.
Česko-slovenská pediatrie, year: 2019, volume: 74, edition: 7
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Targeted resequencing of genes associated with long QT syndrome in Czech patients: two newly identified likely pathogenic variants in previously investigated patient with negative results
Year: 2019, type: Conference abstract
2017
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„Founder“ mutace asociované se syndromem dlouhého QT: Česká republika versus svět
Year: 2017, type: Appeared in Conference without Proceedings
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Klinické a genetické charakteristiky mutace T309I-Kv7.1 asociované se syndromem dlouhého QT
Year: 2017, type: Appeared in Conference without Proceedings
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T309I-Kv7.1 mutation as a feasible founder LQT1 mutation: clinical, genetic and biophysical analysis
Year: 2017, type: Conference abstract
2016
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Clonal cytogenetics changes in progression of multiple myeloma to extramedullary relapse and plasmocellular leukemia: a case report
International Journal of Clinical and Experimental Pathology, year: 2016, volume: 9, edition: 1
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Mutace T309I jako možná „founder„ mutace syndromu dlouhého intervalu QT typu I
Year: 2016, type: Conference abstract