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Autor:
M Loane, J E Given, J Tan, A Reid, D Akhmedzhanova, G Astolfi, I Barišić, N Bertille, L B Bonet, C C Carbonell, O Mokoroa Carollo, A Coi, J Densem, E Draper, E Garne, M Gatt, S V Glinianaia, A Heino, E Den Hond, S Jordan, B Khoshnood, S Kiuru-Kuhlefelt, K Klungsøyr, N Lelong, L R Lutke, A J Neville, L Ostapchuk, A Puccini, A Rissmann, M Santoro, I Scanlon, G Thys, D Tucker, S K Urhoj, H E K de Walle, D Wellesley, O Zurriaga, J K Morris
Publikováno v:
PLoS ONE, Vol 16, Iss 8, p e0256535 (2021)
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 1
Externí odkaz:
https://doaj.org/article/1268a025bf444663ae3263bef99d6df6
