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Article

An MLPA-based strategy for discrete CNV genotyping: CNV-miRNAs as an example.

Human mutation - 1 May 2013

Marcinkowska-Swojak Malgorzata, Uszczynska Barbara, Figlerowicz Marek, Kozlowski Piotr

Abstract excerpt

Copy number variation (CNV) has become well recognized in recent years. It has been estimated that common CNVs account for approximately 10% of the human genome and that they overlap hundreds of genes and other functional genetic elements. Although substantial progress in genome-wide CNV analysis has been made recently, there is still a need for a method that allows precise genotyping of selected CNVs. Here, we...

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PMID: 23381783
DOI: 10.1002/humu.22288

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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