Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in Europe

D Wellesley, Helen Dolk, PA Boyd, M Haeusler, V Nelen, E Garne, B Khoshnood, B Doray, A Rissmann, C Mullaney, E Calzolari, M Bakker, J Salvador, M-C Addor, E Draper, J Rankin, D Tucker

    Research output: Contribution to journalArticle

    72 Citations (Scopus)
    LanguageEnglish
    Pages521-526
    JournalEuropean Journal of Human Genetics
    Volume20
    Issue number5
    DOIs
    Publication statusPublished - 2012

    Cite this

    Wellesley, D ; Dolk, Helen ; Boyd, PA ; Haeusler, M ; Nelen, V ; Garne, E ; Khoshnood, B ; Doray, B ; Rissmann, A ; Mullaney, C ; Calzolari, E ; Bakker, M ; Salvador, J ; Addor, M-C ; Draper, E ; Rankin, J ; Tucker, D. / Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in Europe. In: European Journal of Human Genetics. 2012 ; Vol. 20, No. 5. pp. 521-526.
    @article{ff313b180fbf42fb9bbb2ebce4ecfe56,
    title = "Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in Europe",
    author = "D Wellesley and Helen Dolk and PA Boyd and M Haeusler and V Nelen and E Garne and B Khoshnood and B Doray and A Rissmann and C Mullaney and E Calzolari and M Bakker and J Salvador and M-C Addor and E Draper and J Rankin and D Tucker",
    year = "2012",
    doi = "10.1038/ejhg.2011.246",
    language = "English",
    volume = "20",
    pages = "521--526",
    journal = "European Journal of Human Genetics",
    issn = "1018-4813",
    number = "5",

    }

    Wellesley, D, Dolk, H, Boyd, PA, Haeusler, M, Nelen, V, Garne, E, Khoshnood, B, Doray, B, Rissmann, A, Mullaney, C, Calzolari, E, Bakker, M, Salvador, J, Addor, M-C, Draper, E, Rankin, J & Tucker, D 2012, 'Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in Europe', European Journal of Human Genetics, vol. 20, no. 5, pp. 521-526. https://doi.org/10.1038/ejhg.2011.246

    Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in Europe. / Wellesley, D; Dolk, Helen; Boyd, PA; Haeusler, M; Nelen, V; Garne, E; Khoshnood, B; Doray, B; Rissmann, A; Mullaney, C; Calzolari, E; Bakker, M; Salvador, J; Addor, M-C; Draper, E; Rankin, J; Tucker, D.

    In: European Journal of Human Genetics, Vol. 20, No. 5, 2012, p. 521-526.

    Research output: Contribution to journalArticle

    TY - JOUR

    T1 - Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in Europe

    AU - Wellesley, D

    AU - Dolk, Helen

    AU - Boyd, PA

    AU - Haeusler, M

    AU - Nelen, V

    AU - Garne, E

    AU - Khoshnood, B

    AU - Doray, B

    AU - Rissmann, A

    AU - Mullaney, C

    AU - Calzolari, E

    AU - Bakker, M

    AU - Salvador, J

    AU - Addor, M-C

    AU - Draper, E

    AU - Rankin, J

    AU - Tucker, D

    PY - 2012

    Y1 - 2012

    U2 - 10.1038/ejhg.2011.246

    DO - 10.1038/ejhg.2011.246

    M3 - Article

    VL - 20

    SP - 521

    EP - 526

    JO - European Journal of Human Genetics

    T2 - European Journal of Human Genetics

    JF - European Journal of Human Genetics

    SN - 1018-4813

    IS - 5

    ER -