A sustainable solution for the activities of the European network for surveillance of congenital anomalies: EUROCAT as part of the EU Platform on Rare Diseases Registration

Agnieszka Kinsner‐Ovaskainen(European Commission), Simona Cristina Martin(Joint Research Centre), Anke Rißmann(Otto-von-Guericke-Universität Magdeburg), Maria Loane(University of Ulster), Joan K. Morris(St George's, University of London), David Tucker(UNSW Sydney), Ester Garne(University of Southern Denmark), Monica Lanzoni(Joint Research Centre), Judith Rankin(Cumbria Northumberland Tyne and Wear NHS Foundation Trust), Amanda J. Neville(University of Ferrara), Ciarán Nicholl(Joint Research Centre)
European Journal of Medical Genetics
March 27, 2018
Cited by 71


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