"Panczak, Ale\u0161" . . "S, V" . "5"^^ . "RIV/00064165:_____/12:12456" . "Varianty chromosomu 9 v novorozeneck\u00E9 populaci a jejich klinick\u00FD v\u00FDznam" . "During cytogenetic examination we encounter various cytogenetic abnormalities. Not all of them (like structural or numerical chromosomal aberrations) are simply pathological. So called chromosomal variants are the chromosomal abnormalities, that are not associated with any risks for their carriers. Especially the variants of the heterochromatin area of human chromosome 9 are very common. Although these variants are also believed to be clinically insignificant findings, numerous authors had mentioned possible association of these variants with different types of congenital anomalies. However, in our study we have proved no such association."@en . "Varianty chromosomu 9 v novorozeneck\u00E9 populaci a jejich klinick\u00FD v\u00FDznam"@cs . . . "Varianty chromosomu 9 v novorozeneck\u00E9 populaci a jejich klinick\u00FD v\u00FDznam" . . . "Variants of chromosome 9 in the newborn population and their clinical significance"@en . "V r\u00E1mci cytogenetick\u00E9ho vy\u0161et\u0159en\u00ED se m\u016F\u017Eeme setkat jak s jednozna\u010Dn\u011B patologick\u00FDmi n\u00E1lezy (strukturn\u00ED \u010Di numerick\u00E9 chromosom\u00E1ln\u00ED abnormality), tak i s variantami, kter\u00E9 pro sv\u00E9 nositele v\u011Bt\u0161inou neznamenaj\u00ED \u017E\u00E1dn\u00E9 klinick\u00E9 riziko. Velmi \u010Dasto jsou zachycov\u00E1ny varianty heterochromatinov\u00E9 oblasti chromosomu 9. A\u010Dkoliv jsou dlouh\u00E9 roky pova\u017Eov\u00E1ny za klinicky nev\u00FDznamn\u00E9, \u0159ada autor\u016F popsala mo\u017Enou asociaci t\u011Bchto variant a r\u016Fzn\u00FDch typ\u016F v\u00FDvojov\u00FDch vad. V r\u00E1mci na\u0161\u00ED studie jsme ov\u0161em \u017E\u00E1dnou takovouto asociaci nepotvrdili."@cs . "3"^^ . "12" . "3"^^ . . "177024" . . . . "Varianty chromosomu 9 v novorozeneck\u00E9 populaci a jejich klinick\u00FD v\u00FDznam"@cs . . "karyotype; chromosomes; congenital anomalies; cytogenetic variants"@en . . . "CZ - \u010Cesk\u00E1 republika" . . "Mihalov\u00E1, Romana" . . "Suttrov\u00E1, Eva" . "2" . "Variants of chromosome 9 in the newborn population and their clinical significance"@en . "1211-1600" . "Neonatologick\u00E9 listy" . "RIV/00064165:_____/12:12456!RIV13-MZ0-00064165" . . . . . "[E3730FAEDCFB]" . . "\u0160\u00EDpek, Anton\u00EDn" . "V r\u00E1mci cytogenetick\u00E9ho vy\u0161et\u0159en\u00ED se m\u016F\u017Eeme setkat jak s jednozna\u010Dn\u011B patologick\u00FDmi n\u00E1lezy (strukturn\u00ED \u010Di numerick\u00E9 chromosom\u00E1ln\u00ED abnormality), tak i s variantami, kter\u00E9 pro sv\u00E9 nositele v\u011Bt\u0161inou neznamenaj\u00ED \u017E\u00E1dn\u00E9 klinick\u00E9 riziko. Velmi \u010Dasto jsou zachycov\u00E1ny varianty heterochromatinov\u00E9 oblasti chromosomu 9. A\u010Dkoliv jsou dlouh\u00E9 roky pova\u017Eov\u00E1ny za klinicky nev\u00FDznamn\u00E9, \u0159ada autor\u016F popsala mo\u017Enou asociaci t\u011Bchto variant a r\u016Fzn\u00FDch typ\u016F v\u00FDvojov\u00FDch vad. V r\u00E1mci na\u0161\u00ED studie jsme ov\u0161em \u017E\u00E1dnou takovouto asociaci nepotvrdili." . "Celbov\u00E1, L." .