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Population-based cancer registries for quality-of-life research

✍ Scribed by Thong, Melissa S. Y.; Mols, Floortje; Stein, Kevin D.; Smith, Tenbroeck; Coebergh, Jan-Willem W.; van de Poll-Franse, Lonneke V.

Book ID
120936041
Publisher
John Wiley and Sons
Year
2013
Tongue
English
Weight
189 KB
Volume
119
Category
Article
ISSN
0008-543X

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## Abstract The European Surveillance of Congenital Anomalies (EUROCAT) network of population‐based congenital anomaly registries is an important source of epidemiologic information on congenital anomalies in Europe covering live births, fetal deaths from 20 weeks gestation, and terminations of pre