"Preconceptional, prenatal prevention; US minimarkers; tuberous sclerosis; Y chromosome infertility; intrauterine operations; uropoetic tract defects; IVF+ET improving."@en . "Prekoncep\u010Dn\u00ED a prenat\u00E1ln\u00ED prevence vrozen\u00FDch vad a d\u011Bdi\u010Dn\u00FDch onemocn\u011Bn\u00ED s jejich intrauterinn\u00EDm a postnat\u00E1ln\u00EDm \u0159e\u0161en\u00EDm" . "1"^^ . "Zdokonalen\u00ED klinicko-genetick\u00FDch metod reproduk\u010Dn\u00ED genetiky. Molekul\u00E1rn\u00ED genetick\u00E1 diagnostika. Zdokonalen\u00ED embryologick\u00FDch metod mimot\u011Bln\u00EDho oplozen\u00ED. Diagnostika idiopatick\u00E9 ment\u00E1ln\u00ED retardace."@en . . "2"^^ . "Zdokonalen\u00ED klinicko-genetick\u00FDch metod reproduk\u010Dn\u00ED genetiky. Molekul\u00E1rn\u00ED genetick\u00E1 diagnostika. Zdokonalen\u00ED embryologick\u00FDch metod mimot\u011Bln\u00EDho oplozen\u00ED. Diagnostika idiopatick\u00E9 ment\u00E1ln\u00ED retardace."@cs . . . "0"^^ . "2008-06-02+02:00"^^ . . . "27"^^ . "Sn\u00ED\u017Een\u00ED v\u00FDskytu vrozen\u00FDch v\u00FDvojov\u00FDch vad a d\u011Bdi\u010Dn\u00FDch onemocn\u011Bn\u00ED v populaci. Jejich diagnostika v \u010Dasn\u00E9m stadiu t\u011Bhotenstv\u00ED \u010Di obdob\u00ED prekoncep\u010Dn\u00EDm - DNA anal\u00FDzou a sonografick\u00FDmi markery. Sn\u00ED\u017Een\u00ED rizika v\u00EDce\u010Detn\u00FDch t\u011Bhotenstv\u00ED v programu IVF+ET.P\u0159esun diagnostiky do I. trimestru gravidity a anal\u00FDza defekt\u016F na bun\u011B\u010Dn\u00E9 \u00FArovni DNA probami. Sonografick\u00E1 diagnostika chromozom\u00E1ln\u00EDch aberac\u00ED tzv. minimarkery. Detekce primer\u016F v oblasti Y chromozom\u016F spojen\u00FDch s poruchou plodnosti.Detekce subtelomerick\u00FDch chromozom\u00E1ln\u00EDch abnormalit u pacient\u016F s idiopatickou ment\u00E1ln\u00ED retardac\u00ED FISH technikou. DNA diagnostika tuberozn\u00ED skler\u00F3zy. Mo\u017Enosti a efektivita intrauterinn\u00EDch operativn\u00EDch z\u00E1krok\u016F u vrozen\u00FDch poruch uropoetick\u00E9ho traktu.Sn\u00ED\u017Een\u00ED rizika v\u00EDce\u010Detn\u00FDch t\u011Bhotenstv\u00ED v r\u00E1mci programu IVF+ET p\u0159enosem pouze dvou embry\u00ED p\u0159i zachov\u00E1n\u00ED dosavadn\u00ED efektivity. Jde o stimulaci, zisk funk\u010Dn\u011B zdatn\u00FDch oocyt\u016F, jejich fertilizaci a kultivaci a\u017E do vy\u0161\u0161\u00EDch st\u00E1di\u00ED v\u00FDvoje blastocysty." . . "12"^^ . . . "The lowering of the congenital defects and inherited diseases onset in population. Early diagnosis in the I. trimester or preconceptionally by DNA analysis and US markers. The risk lowering of the multiple gravidities at the IVF+ET programme.Transfer of congenital defects and inherited diseases into the I. trimester of pregnancy and DNA analysis of these conditions on cell level. Sonography of chromosomal aberrations by minimarkers. Dysfunctions of fertility caused by Y chromosome primers.Detection of subtelomeric chromosomal aberrations at patiens with idiopathic mental retardation by FISH. DNA analysis of the tuberous sclerosis. Options and effectivity of intrauterine operations at the uropoetic tract congenital defects.Risk lowering of multiple gravidities at IVF+ET by transfer 2 embryos only at the maintenance effectivity. Stimulation, functionally efficient oocyts acquisition, their fertilization and cultivation to the stage of the higher development of blastocysts."@en . . . "Preconceptional and prenatal prevention of the congenital defects and inherited diseases with their intrauterine and postnatal management"@en . . "27"^^ . . . . . . . . "0"^^ .