Total number of publications: 202
2012
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Clinical characteristics of 30 Czech families with long QT syndrome and KCNQ1 and KCNH2 gene mutations: importance of exercise testing
Journal of Electrocardiology, year: 2012, volume: 45, edition: 6, DOI
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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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Genodermatózy
Year: 2012, type: Conference abstract
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Li-Fraumeni syndrom – návrh komplexní preventivní péče o nosiče TP53 mutace s použitím celotělové magnetické rezonance
Klinická onkologie, year: 2012, volume: 2012, edition: 25
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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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Několik poznámek ke genetickému podkladu kožních chorob
Referátový výběr z dermatovenerologie, year: 2012, volume: 54, edition: 1
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Pertusse u kojence s nepoznanou cystickou fibrózou
Klinická mikrobiologie a infekční lékařství, year: 2012, volume: 18, edition: 6
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Sperm meiotic segregation, aneuploidy and high risk of delivering an affected offspring in carriers of non-Robertsonian translocation t(13;15)
Journal of Assisted Reproduction and Genetics, year: 2012, volume: 29/2012, edition: 7, DOI
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The effect of the swim-up and hyaluronan-binding methods on the frequency of abnormal spermatozoa detected by FISH and SCSA in carriers of balanced chromosomal translocations
HUMAN REPRODUCTION, year: 2012, volume: 27, edition: 3, DOI
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Two years experience with CF newborn screening in University Hospital Brno
Year: 2012, type: Conference abstract