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: 69
2017
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Význam a využití NGS v diagnostice dědičných trombocytopenií.
Year: 2017, type: Conference abstract
2015
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Molecular genetic diagnostics of congenital adrenal hyperplasia in the Czech republic.
Year: 2015, type: Conference abstract
2014
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The extension of molecular genetic diagnostics of congenital adrenal hyperplasia in the Czech Republic
Year: 2014, type: Conference abstract
2013
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Molekulární diagnostika kongenitální adrenální hyperplázie - rozšíření spektra vyšetření
Year: 2013, type:
2012
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Lessons learned from 5 years of newborn screening for congenital adrenal hyperplasia in the Czech Republic: 17-hydroxyprogesterone, genotypes, and screening performance
European Journal of Paediatrics, year: 2012, volume: 171, edition: 6, DOI
2011
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Chimeric CYP21A1P/CYP21A2 genes identified in Czech patients with congenital adrenal hyperplasia
European Journal of Medical Genetics, year: 2011, volume: 54, edition: 2, DOI
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Identification of CYP21A2 mutations in Czech patients with 21-hydroxylase deficiency - structural analysis of the chimeric CYP21A1P/CYP21A2 gene.
Year: 2011, type: Conference abstract
2010
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Molekulárně genetická analýza kongenitální adrenální hyperplasie (deficit 21- a 11-beta-hydroxylázy).
Year: 2010, type: Conference abstract
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Molekulárně genetická diagnostika Pompeho choroby
Year: 2010, type:
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The molecular – genetic analysis of congenital adrenal hyperplasia in Czech population (21- and 11-β-hydroxylase deficienty).
Year: 2010, type: Conference abstract