Cohort profile: the National Congenital Anomaly Registration Dataset in England

Purpose The National Congenital Anomaly and Rare Disease Registration Service (NCARDRS), part of National Disease Registration Service in National Health Service England, quality assures, curates and analyses individual data on the pregnancies, fetuses, babies, children and adults with congenital an...

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書誌詳細

主要な著者:	Danielle Martin, Sarah Stevens, John Broggio, Chloe Johnson, Kate M Fleming, Ben Wreyford, Sylvia Stoianova, Gabriella Melis, Ewoma Obaro, Jennifer M. Broughan, Kay Randall, Nicholas Aldridge, Donna Gibbard
フォーマット:	Artigo
言語:	Inglês
出版事項:	BMJ Publishing Group 2024-01-01
シリーズ:	BMJ Open
オンライン･アクセス:	https://bmjopen.bmj.com/content/14/1/e077743.full
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