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National Congenital Anomaly and Rare Disease Registration Service. Congenital anomaly statistics

Online Catalogue | Official Publications | Non-Parliamentary Official Publications | Department of Health and Social Care (DHSC) |  National Congenital Anomaly and Rare Disease Registration Service. Congenital anomaly statistics


National Congenital Anomaly and Rare Disease Registration Service. Congenital anomaly statistics 2020 National Congenital Anomaly and Rare Disease Registration Service. Congenital anomaly statistics 2020 is in stock now

National Congenital Anomaly and Rare Disease Registration Service. Congenital anomaly statistics 2020


14.00
This publication contains information on congenital anomalies in babies delivered in England in 2020. It includes this report showing key findings, spreadsheet tables with more detailed estimates and a methodology document.

The National Congenital Anomaly and Rare Disease Registration Service (NCARDRS) is a comprehensive registration service that collects and quality assures data on congenital anomalies and rare diseases in England.

This is the sixth annual congenital anomaly statistics report released by NCARDRS and the third report to contain national data for the whole of England. The report contains information on congenital anomalies detected in babies delivered between 1 January and 31 December 2020.

Spreadsheet data tables with detailed estimates are attached to this report; these can be found in the accompanying CD-ROM disk. 
ISBN
9781804921227
Author
NHS Digital
Published by
Dandy Booksellers Ltd
Publication Date
6 December 2022
Edition
2020
Format
Paperback
Extent
52 pages plus CD-ROM
Dimensions
A4 (210 x 297 mm)
Approx Weight
0.21 kg
HS Code
490199






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