RNDr. Iveta Valášková, Ph.D.
Assistant professor, Institute of Medical Genetics and Genomics
Phone: | +420 532 23 4718 |
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E‑mail: |
social and academic networks: |
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Total number of publications: 73
2014
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Instrumentální technika. Obor zdravotní laborant
Year: 2014, type:
2013
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A familial case of alveolar capillary dysplasia with misalignment of pulmonary veins supports paternal imprinting of FOXF1 in human
European Journal of Human Genetics, year: 2013, volume: 21, edition: 4, DOI
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Alveolární kapilární dysplazie - familiární výskyt
Year: 2013, type: Appeared in Conference without Proceedings
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Novel FOXF1 Mutations in Sporadic and Familial Cases of Alveolar Capillary Dysplasia with Misaligned Pulmonary Veins Imply a Role for its DNA Binding Domain
Human Mutation, year: 2013, volume: 34, edition: 6, DOI
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Towards Clinical Molecular Diagnosis of Inherited Cardiac Conditions: A Comparison of Bench-Top Genome DNA Sequencers
PLoS One, year: 2013, volume: 8, edition: 7, DOI
2012
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Detection of the mutation D1152H in the CFTR gene in University Hospital Brno, Czech Republic
Year: 2012, type: Conference abstract
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Molecular Genetic Analysis of Fetal Tissues from a Family Affected by Myotonic Dystrophy
Česká a slovenská neurologie a neurochirurgie, year: 2012, volume: 75, edition: 6
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Mutation analysis of RyR2 gene in patients after arrhythmic storm
Cor et Vasa, year: 2012, volume: 54, edition: 2, DOI
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Two years experience with CF newborn screening in University Hospital Brno
Year: 2012, type: Conference abstract
2011
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Analysis of HGG-02 cell line with loss of EGFR gene copy derived from childhood glioblastoma multirme.
Year: 2011, type: Conference abstract