The "Geneticisation" of Disease Stigma
Creator
Savulescu, Julian
Kerin, Jacinta
Bibliographic Citation
Lancet 1999 December; 354(supplement 4): SIV16
Permanent Link
Find Full Text at Georgetown University LibraryFull Text from Publisher
http://hdl.handle.net/10822/507057
Date
2000-02-07Collections
Metadata
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Infectious Disease Ethics: Limiting Liberty in Contexts of Contagion
Selgelid, Michael J.; Mclean, Angela R.; Arinaminpathy, Nimalan; Savulescu, Julian (2009-06) -
"You're one of us now": young people describe their experiences of predictive genetic testing for Huntington disease (HD) and familial adenomatous polyposis (FAP)
Duncan, Rony E.; Gillam, Lynn; Savulescu, Julian; Williamson, Robert; Rogers, John G.; Delatycki, Martin B. (2008-02-15) -
Prenatal diagnosis requests for Huntington's disease when the father is at risk and does not want to know his genetic status: clinical, legal, and ethical viewpoints
Tassicker, Ros; Savulescu, Julian; Skene, Loane; Marshall, Pam; Fitzgerald, Lara; Delatycki, Martin B. (2003-02-08)Summary points: When the father is at 50% risk of having Huntington's disease, there is a 1 in 4 chance that prenatal testing will show that he has the mutation and will develop the disease; Testing for Huntington's disease ...