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1. A doubling. SEE ALSO: reduplication. 2. Inclusion of two copies of the same genetic material in a genome; an important step in diversification of genomes, as in the evolution of the (nonallelic) hemoglobin chains from a common ancestor. SYN: gene d.. [L. duplicatio, a doubling, fr. duplico, to double]
- d. of chromosomes a chromosome aberration resulting from unequal crossing over or exchange of segments between two homologous chromosomes; one chromosome of the pair loses a small segment, while the other gains this segment; the chromosome gaining the segment has undergone d. while its homologue has undergone deletion. See hemoglobin Lepore.
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1) the act or process of duplicating: the quality or state of being duplicated
2) a part of a chromosome in which the genetic material is repeated also the process of forming a duplication
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du·pli·ca·tion (doo″plĭ-kaґshən) [L. duplicatio doubling] 1. the act or process of doubling, or the state of being doubled. 2. in genetics, the presence in the genome of additional genetic material (a chromosome or segment of one, a gene or part of one). See also repeat. 3. a doubling of parts, which may be connected at some point, the extra part may be a mirror image of the other. See also conjoined twins, under twin. Called also duplicitas and reduplication.Medical dictionary. 2011.