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- W4245733838 abstract "Copy number variations (CNVs) currently are most often understood as submicroscopic gains or losses of chromosomal material, either connected with a disease or just one of the many possible genetic variants in man. However decades ago, besides such submicroscopic CNVs, chromosome analysis revealed the existence of cytogenetic visible copy number variations (CG-CNVs). In this chapter a short outline of cytogenetic history is given, highlighting the first detection and overinterpretation and possible meanings of CG-CNVs. Also heterochromatic and euchromatic CG-CNVs are distinguished from submicroscopic CNVs and some specific features of each group are introduced." @default.
- W4245733838 created "2022-05-12" @default.
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- W4245733838 date "2014-01-01" @default.
- W4245733838 modified "2023-09-26" @default.
- W4245733838 title "Introduction" @default.
- W4245733838 doi "https://doi.org/10.1016/b978-0-12-404631-3.00001-5" @default.
- W4245733838 hasPublicationYear "2014" @default.
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