Total number of publications: 200
2008
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Molecular genetic identification of the major cyp2d6 alleles and utilization in psychiatric treatment of depression
The International Journal of Neuropsychopharmacology, year: 2008, volume: 11, edition: suppl.1
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Molekulárně genetická analýza Rb1 genu u dětí s retinoblastomem.
Year: 2008, type: Conference abstract
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Molekulárně genetická diagnostika Epidermolysis bullosa congenita v ČR
Year: 2008, type: Conference abstract
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Mutation analysis of candidate genes SCN1B, KCND3 and ANK2 in patients with clinical diagnosis of Long QT syndrome.
Physiological Research, year: 2008, volume: 57/2008, edition: 6
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Mutation Analysis of Dystrophic Epidermolysis Bullosa in the Czech Republic
Year: 2008, type: Conference abstract
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Mutation Analysis of Epidermolysis Bullosa in the Czech Republic
Year: 2008, type: Conference abstract
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Mutation analysis of ion channel genes in sudden death survivors - a pilot study
Giornale Italiano di Aritmologia e Cardiostimolazione, year: 2008, volume: 11, edition: 4
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První případ prenatální diagnostiky v rodině s Epidermolysis bullosa simplex- Dowling-Meara
Česko - Slovenská Pediatrie, year: 2008, volume: 63, edition: 7.-8.
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Spinal muscular atrophy in University Hospital Brno, Czech Republic – Genetic counselling DNA analysis
Year: 2008, type: Conference abstract
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Variability of clinical symptoms in patients with genetically confirmed diagnosis of long QT syndrome.
Slovenska kardiologia, year: 2008, volume: ř, edition: suppl.1