Linking a European cohort of children born with congenital anomalies to vital statistics and mortality records: A EUROlinkCAT study

EUROCAT is a European network of population-based congenital anomaly (CA) registries. Twenty-one registries agreed to participate in the EUROlinkCAT study to determine if reliable information on the survival of children born with a major CA between 1995 and 2014 can be obtained through linkage to na...

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Detalles Bibliográficos
Autores principales: Loane, M., Given, J. E., Tan, J., Reid, A., Akhmedzhanova, D., Astolfi, G., Barišić, I., Bertille, N., Bonet, L. B., Carbonell, C. C., Carollo, O. Mokoroa, Coi, A., Densem, J., Draper, E., Garne, E., Gatt, M., Glinianaia, S. V., Heino, A., Hond, E. Den, Jordan, S., Khoshnood, B., Kiuru-Kuhlefelt, S., Klungsøyr, K., Lelong, N., Lutke, L. R., Neville, A. J., Ostapchuk, L., Puccini, A., Rissmann, A., Santoro, M., Scanlon, I., Thys, G., Tucker, D., Urhoj, S. K., de Walle, H. E. K., Wellesley, D., Zurriaga, O., Morris, J. K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8396745/
https://www.ncbi.nlm.nih.gov/pubmed/34449798
http://dx.doi.org/10.1371/journal.pone.0256535

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