Paper 6: EUROCAT member registries: organization and activities

Ruth Greenlees; A Neville; MC Addor; E Amar; L Arriola; M Bakker; I Barisic; PA Boyd; E Calzolari; B Doray; E Draper; [Unknown] et al

doi:10.1002/bdra.20775

Paper 6: EUROCAT member registries: organization and activities

Ruth Greenlees
, A Neville
, MC Addor
, E Amar
, L Arriola
, M Bakker
, I Barisic
, PA Boyd
, E Calzolari
, B Doray
, E Draper
, [Unknown] et al

Research output: Contribution to journal › Article › peer-review

114 Citations (Scopus)

Abstract

EUROCAT is a network of population-based congenital anomaly registries providing standardized epidemiologic information on congenital anomalies in Europe. There are three types of EUROCAT membership: full, associate, or affiliate. Full member registries send individual records of all congenital anomalies covered by their region. Associate members transmit aggregate case counts for each EUROCAT anomaly subgroup by year and by type of birth. This article describes the organization and activities of each of the current 29 full member and 6 associate member registries of EUROCAT.

Original language	English
Pages (from-to)	S51-S100
Journal	Birth Defects Research (Part A)
Volume	91
Issue number	1
DOIs	https://doi.org/10.1002/bdra.20775
Publication status	Published (in print/issue) - 2011

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10.1002/bdra.20775

http://www.ncbi.nlm.nih.gov/pubmed/21381185

Cite this

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abstract = "EUROCAT is a network of population-based congenital anomaly registries providing standardized epidemiologic information on congenital anomalies in Europe. There are three types of EUROCAT membership: full, associate, or affiliate. Full member registries send individual records of all congenital anomalies covered by their region. Associate members transmit aggregate case counts for each EUROCAT anomaly subgroup by year and by type of birth. This article describes the organization and activities of each of the current 29 full member and 6 associate member registries of EUROCAT.",

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AU - Neville, A

AU - Addor, MC

AU - Amar, E

AU - Arriola, L

AU - Bakker, M

AU - Barisic, I

AU - Boyd, PA

AU - Calzolari, E

AU - Doray, B

AU - Draper, E

AU - et al, [Unknown]

PY - 2011

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AB - EUROCAT is a network of population-based congenital anomaly registries providing standardized epidemiologic information on congenital anomalies in Europe. There are three types of EUROCAT membership: full, associate, or affiliate. Full member registries send individual records of all congenital anomalies covered by their region. Associate members transmit aggregate case counts for each EUROCAT anomaly subgroup by year and by type of birth. This article describes the organization and activities of each of the current 29 full member and 6 associate member registries of EUROCAT.

U2 - 10.1002/bdra.20775

DO - 10.1002/bdra.20775

M3 - Article

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SP - S51-S100

JO - Birth Defects Research (Part A)

JF - Birth Defects Research (Part A)

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Paper 6: EUROCAT member registries: organization and activities

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