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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Detaylı Bibliyografya
Asıl Yazarlar:	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
Materyal Türü:	Artigo
Dil:	Inglês
Baskı/Yayın Bilgisi:	BMJ Publishing Group 2024-01-01
Seri Bilgileri:	BMJ Open
Online Erişim:	https://bmjopen.bmj.com/content/14/1/e077743.full
Etiketler:	Etiketle Etiket eklenmemiş, İlk siz ekleyin!

Cohort profile: the National Congenital Anomaly Registration Dataset in England

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