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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| Hauptverfasser: | , , , , , , , , , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
BMJ Publishing Group
2024-01-01
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| Schriftenreihe: | BMJ Open |
| Online-Zugang: | https://bmjopen.bmj.com/content/14/1/e077743.full |
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