Ing. Zuzana Vrzalová, Ph.D.
Research specialist, Genomics Core Facility
Office: bldg. E35/255
Kamenice 753/5
625 00 Brno
Phone: | +420 549 49 6997 |
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E‑mail: |
social and academic networks: |
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Total number of publications: 70
2023
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Korelace fenotypu a genotypu u dvou rodin s hereditární sférocytózou.
Year: 2023, type: Conference abstract
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Nově identifikovaná varianta v genu CYCS u rodiny s trombocytopenií typu 4 a její funkční dopad.
Year: 2023, type: Conference abstract
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Phenotype-genotype corellation in two families with hereditary spherocytosis.
Year: 2023, type: Conference abstract
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Rozsáhlá delece 22q12 u pacienta s oboustranným Schwannomem, mentální retardací, percepční sluchovou poruchou a epilepsií.
Year: 2023, type: Conference abstract
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Varianta v genu CYCS způsobující trombocytopenii 4 zvyšuje kaspázovou aktivitu.
Year: 2023, type: Conference abstract
2022
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A GP1BA Variant in a Czech Family with Monoallelic Bernard-Soulier Syndrome
International Journal of Molecular Sciences, year: 2022, volume: 23, edition: 2, DOI
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Analysis of ANKRD26 gene 5´UTR variant in a cohort of Czech patients with suspected hereditary hematological disorder
Year: 2022, type: Conference abstract
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ANALYSIS OF ANKRD26 GENE 5'UTR VARIANTS IN A COHORT OF CZECH PATIENTS WITH SUSPECTED HEREDITARY HEMATOLOGICAL DISORDER
Year: 2022, type: Conference abstract
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Delece 22q12 u pacienta s bilaterálním schwannomem zachycená kombinací metod NGS, MLPA a array-CGH.
Year: 2022, type: Conference abstract
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Genetická diagnostika familiárních onemocnění krvetvorby a stanovení jejich funkčního dopadu.
Year: 2022, type: Conference abstract