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Description
  • The term %22copy number variation/variant%22 (CNV) denotes a DNA sequence with a magnitude of 1 kb at least which is differently represented among individuals based on its deletion or duplication. Since 2008, multiple studies have reported copy number variations in schizophrenia, and they seem to fill in a gap in our knowledge on the genetic background of schizophrenia.
  • The term %22copy number variation/variant%22 (CNV) denotes a DNA sequence with a magnitude of 1 kb at least which is differently represented among individuals based on its deletion or duplication. Since 2008, multiple studies have reported copy number variations in schizophrenia, and they seem to fill in a gap in our knowledge on the genetic background of schizophrenia. (en)
Title
  • Genomic copy number variations: A breakthrough in our knowledge on schizophrenia etiology?
  • Genomic copy number variations: A breakthrough in our knowledge on schizophrenia etiology? (en)
skos:prefLabel
  • Genomic copy number variations: A breakthrough in our knowledge on schizophrenia etiology?
  • Genomic copy number variations: A breakthrough in our knowledge on schizophrenia etiology? (en)
skos:notation
  • RIV/61988987:17110/12:A13017K4!RIV13-MSM-17110___
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  • RIV/61988987:17110/12:A13017K4
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http://linked.open.../riv/klicovaSlova
  • schizophrenia; genetics; DNA copy number variations; gene expression; population characteristics (en)
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  • SE - Švédské království
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  • 33
http://linked.open...iv/tvurceVysledku
  • Hosák, Ladislav
  • Hosáková, Jiřina
  • Šilhán, Petr
issn
  • 0172-780X
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  • 17110
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