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Article

A parallel SNP array study of genomic aberrations associated with mental retardation in patients and general population in Estonia.

European journal of medical genetics - 1 Jan 2000

Männik Katrin, Parkel Sven, Palta Priit, Zilina Olga, Puusepp Helen, Esko Tõnu, Mägi Reedik, Nõukas Margit, Veidenberg Andres, Nelis Mari, Metspalu Andres, Remm Maido, Ounap Katrin, Kurg Ants

Abstract excerpt

The increasing use of whole-genome array screening has revealed the important role of DNA copy-number variations in the pathogenesis of neurodevelopmental disorders and several recurrent genomic disorders have been defined during recent years. However, some variants considered to be pathogenic ha...

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Identifiers

PMID: 21112420
DOI: 10.1016/j.ejmg.2010.11.005

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-21112420-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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