Survey of informed consent for registration of congenital anomalies in Europe
about
Community attitudes to the collection and use of identifiable data for health research--is it an invasion of privacy?The European data protection legislation and its consequences for public health monitoring: a plea for actionPassive consent for clinical research in the age of HIPAA.Detecting congenital malformations - Lessons learned from the Mpepu study, Botswana.
P2860
Survey of informed consent for registration of congenital anomalies in Europe
description
2005 nî lūn-bûn
@nan
2005 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Survey of informed consent for registration of congenital anomalies in Europe
@ast
Survey of informed consent for registration of congenital anomalies in Europe
@en
type
label
Survey of informed consent for registration of congenital anomalies in Europe
@ast
Survey of informed consent for registration of congenital anomalies in Europe
@en
prefLabel
Survey of informed consent for registration of congenital anomalies in Europe
@ast
Survey of informed consent for registration of congenital anomalies in Europe
@en
P2093
P2860
P356
P1433
P1476
Survey of informed consent for registration of congenital anomalies in Europe
@en
P2093
Annukka Ritvanen
Araceli Busby
David Stone
Helen Dolk
Hermien De Walle
Isolina Riaño-Galán
Miriam Gatt
Nicola Armstrong
Robert McDonnell
Vera Nelen
P2860
P304
P356
10.1136/BMJ.331.7509.140
P407
P577
2005-07-01T00:00:00Z