What are the limits of the duty of care? The case of clinical genetics

被引:3
作者
Borry, Paul [1 ]
Dierickx, Kris [1 ]
机构
[1] Katholieke Univ Leuven, Ctr Biomed Eth & Law, B-3000 Louvain, Belgium
关键词
D O I
10.2217/17410541.5.2.101
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
引用
收藏
页码:101 / 104
页数:4
相关论文
共 40 条
[1]  
Axworthy D, 1996, LANCET, V347, P1443
[2]   UPTAKE OF CYSTIC-FIBROSIS TESTING IN PRIMARY-CARE - SUPPLY PUSH OR DEMAND PULL [J].
BEKKER, H ;
MODELL, M ;
DENNISS, G ;
SILVER, A ;
MATHEW, C ;
BOBROW, M ;
MARTEAU, T .
BRITISH MEDICAL JOURNAL, 1993, 306 (6892) :1584-1586
[3]   THE IMPACT OF POPULATION-BASED SCREENING FOR CARRIERS OF CYSTIC-FIBROSIS [J].
BEKKER, H ;
DENNISS, G ;
MODELL, M ;
BOBROW, M ;
MARTEAU, T .
JOURNAL OF MEDICAL GENETICS, 1994, 31 (05) :364-368
[4]   Carrier testing in minors: a systematic review of guidelines and position papers [J].
Borry, P ;
Fryns, JP ;
Schotsmans, P ;
Dierickx, K .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2006, 14 (02) :133-138
[5]   Attitudes regarding predictive genetic testing in minors: A survey of European clinical geneticists [J].
Borry, Pascal ;
Goffin, Tom ;
Nys, Herman ;
Dierickx, Kris .
AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS, 2008, 148C (01) :78-83
[6]   Attitudes regarding carrier testing in incompetent children: a survey of European clinical geneticists [J].
Borry, Pascal ;
Goffin, Tom ;
Nys, Herman ;
Dierickx, Kris .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2007, 15 (12) :1211-1217
[7]  
BORRY R, 2007, J MED ETHICS IN PRES
[8]  
Callanan NP, 1999, GENET MED, V1, P323
[9]   Genetic counseling and neonatal screening for cystic fibrosis: An assessment of the communication process [J].
Ciske, DJ ;
Haavisto, A ;
Laxova, A ;
Rock, LZM ;
Farrell, PM .
PEDIATRICS, 2001, 107 (04) :699-705
[10]   Genetic professionals' reports of nondisclosure of genetic risk information within families [J].
Clarke, A ;
Richards, M ;
Kerzin-Storrar, L ;
Halliday, J ;
Young, MA ;
Simpson, SA ;
Featherstone, K ;
Forrest, K ;
Lucassen, A ;
Morrison, PJ ;
Quarrell, OWJ ;
Stewart, H .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2005, 13 (05) :556-562