Total number of publications: 201
2012
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Unique Combination of 22q11 and 14qter Microdeletion Syndromes Detected Using Oligonucleotide Array-CGH
Molecular Syndromology, year: 2012, volume: 2011;2, edition: No. 2, DOI
2011
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Analysis of chromosomal aberrations in patients with mental retardation using array-CGH technique: a single Czech Centre experience
Folia biologica, year: 2011, volume: 2011, edition: 57 No.5
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Deletion of 9p associated with sex reversal: clinical and molecular-cytogenetic analysis of patients
Year: 2011
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Familiální výskyt balancované a nebalancované formy translokace t(1;12) v rodině se dvěma postižnými dětmi
Year: 2011, type: Conference abstract
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Molekulárně-genetická diagnostika genodermatóz.
Year: 2011, type: Conference abstract
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Molekulární diagnostika genu RB1 u dětí s Retinoblastomeme.
Year: 2011
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Mutation Analysis Ion Channel Genes Ventricular Fibrillation Survivors with Coronary Artery Disease
PACE-PACING AND CLINICAL ELECTROPHYSIOLOGY, year: 2011, volume: 34, edition: 6, DOI
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Rare Constitutional Chromosomal Rearrangements Found In Three Probands
Year: 2011, type: Conference abstract
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Sperm and embryo analysis of similar t(7;10) translocations transmitted in two families
Fertility and Sterility, year: 2011, volume: 96, edition: 1, DOI
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Vnitřní lékařství
Year: 2011, edition: 1.vyd., number of pages: 1788 s.