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Holt Oram syndrome: a registry-based study in Europe

Academic Article
Publication Date:
2014
abstract:
Methods: The study was based on data collected during 1990-2011 by 34 registries. The registries are population-based and use multiple sources of information to collect data on all types of birth using standardized definitions, methodology and coding. Diagnostic criteria for inclusion in the study were the presence of radial ray abnormalities and congenital heart disease (CHD), or the presence of either radial ray anomaly or CHD, with family history of HOS.
Iris type:
01.01 Articolo in rivista
Keywords:
Holt Oram syndrome; Congenital anomalies; Prenatal diagnosis; Epidemiology; Europe
List of contributors:
Pierini, Anna
Authors of the University:
PIERINI ANNA
Handle:
https://iris.cnr.it/handle/20.500.14243/253485
Published in:
ORPHANET JOURNAL OF RARE DISEASES
Journal
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