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 journalArticle

    82 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.
    LanguageEnglish
    PagesS51-S100
    JournalBirth Defects Research (Part A)
    Volume91
    Issue number1
    DOIs
    Publication statusPublished - 2011

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    Greenlees, R., Neville, A., Addor, MC., Amar, E., Arriola, L., Bakker, M., ... et al, U. (2011). Paper 6: EUROCAT member registries: organization and activities. Birth Defects Research (Part A), 91(1), S51-S100. https://doi.org/10.1002/bdra.20775
    Greenlees, Ruth ; Neville, A ; Addor, MC ; Amar, E ; Arriola, L ; Bakker, M ; Barisic, I ; Boyd, PA ; Calzolari, E ; Doray, B ; Draper, E ; et al, [Unknown]. / Paper 6: EUROCAT member registries: organization and activities. In: Birth Defects Research (Part A). 2011 ; Vol. 91, No. 1. pp. S51-S100.
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    title = "Paper 6: EUROCAT member registries: organization and activities",
    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.",
    author = "Ruth Greenlees and A Neville and MC Addor and E Amar and L Arriola and M Bakker and I Barisic and PA Boyd and E Calzolari and B Doray and E Draper and {et al}, [Unknown]",
    year = "2011",
    doi = "10.1002/bdra.20775",
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    Greenlees, R, Neville, A, Addor, MC, Amar, E, Arriola, L, Bakker, M, Barisic, I, Boyd, PA, Calzolari, E, Doray, B, Draper, E & et al, U 2011, 'Paper 6: EUROCAT member registries: organization and activities', Birth Defects Research (Part A), vol. 91, no. 1, pp. S51-S100. https://doi.org/10.1002/bdra.20775

    Paper 6: EUROCAT member registries: organization and activities. / Greenlees, Ruth; Neville, A; Addor, MC; Amar, E; Arriola, L; Bakker, M; Barisic, I; Boyd, PA; Calzolari, E; Doray, B; Draper, E; et al, [Unknown].

    In: Birth Defects Research (Part A), Vol. 91, No. 1, 2011, p. S51-S100.

    Research output: Contribution to journalArticle

    TY - JOUR

    T1 - Paper 6: EUROCAT member registries: organization and activities

    AU - Greenlees, Ruth

    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]

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    N2 - 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.

    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

    VL - 91

    SP - S51-S100

    JO - Birth Defects Research Part A: Clinical and Molecular Teratology

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    JF - Birth Defects Research Part A: Clinical and Molecular Teratology

    SN - 1542-0752

    IS - 1

    ER -

    Greenlees R, Neville A, Addor MC, Amar E, Arriola L, Bakker M et al. Paper 6: EUROCAT member registries: organization and activities. Birth Defects Research (Part A). 2011;91(1):S51-S100. https://doi.org/10.1002/bdra.20775