Paper 1: The EUROCAT network--organization and processes.

  title={Paper 1: The EUROCAT network--organization and processes.},
  author={Patricia Anne Boyd and Martin C H Haeusler and Ingeborg Bari{\vs}i{\'c} and Maria A Loane and Ester Garne and Helen Dolk},
  journal={Birth defects research. Part A, Clinical and molecular teratology},
  volume={91 Suppl 1},
The European Surveillance of Congenital Anomalies (EUROCAT) is a network of population-based congenital anomaly registries in Europe, funded by the European Union, which has been in operation for more than 30 years. It currently surveys more than 1.7 million births per year, including 31% of births in the European Union, and includes almost all population-based European congenital anomaly registries as its members. EUROCAT member registries collect data, ascertained from multiple sources, on… CONTINUE READING