Greenlees, Ruth, Neville, A, Addor, MC, Amar, E, Arriola, L, Bakker, M, Barisic, I, Boyd, PA, Calzolari, E, Doray, B, Draper, E and et al, . (2011) Paper 6: EUROCAT member registries: organization and activities. Birth Defects Research (Part A), 91 (1). S51-S100. [Journal article]
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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.
|Item Type:||Journal article|
|Faculties and Schools:||Faculty of Life and Health Sciences|
Faculty of Life and Health Sciences > School of Nursing
|Research Institutes and Groups:||Institute of Nursing and Health Research|
Institute of Nursing and Health Research > Maternal, Fetal and Infant Research
|Deposited By:||Mrs Barbra Webber|
|Deposited On:||18 Jun 2012 11:42|
|Last Modified:||18 Jun 2012 11:42|
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