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

    81 Citations (Scopus)
    Original languageEnglish
    Pages (from-to)521-526
    JournalEuropean Journal of Human Genetics
    Volume20
    Issue number5
    DOIs
    Publication statusPublished - 2012

    Cite this

    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, 20(5), 521-526. https://doi.org/10.1038/ejhg.2011.246