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Article

Contribution of de novo and inherited rare CNVs to very preterm birth.

Journal of medical genetics - 1 Aug 2020

Wong Hilary S, Wadon Megan, Evans Alexandra, Kirov George, Modi Neena, O'Donovan Michael C, Thapar Anita

Abstract excerpt

BACKGROUND: The genomic contribution to adverse health sequelae in babies born very preterm (<32 weeks' gestation) is unknown. We conducted an investigation of rare CNVs in infants born very preterm as part of a study to determine the feasibility and acceptability of a larger, well-powered genome-wide investigation in the UK, with follow-up using linked National Health Service records and DNA storage for...

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Identifiers

PMID: 32051258
DOI: 10.1136/jmedgenet-2019-106619

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