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id:"swepub:oai:lup.lub.lu.se:4d3ac8d5-cf0e-4f5b-be06-e67195b6e3dd"
 

Sökning: id:"swepub:oai:lup.lub.lu.se:4d3ac8d5-cf0e-4f5b-be06-e67195b6e3dd" > Provision of geneti...

LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00004066naa a2200433 4500
001oai:lup.lub.lu.se:4d3ac8d5-cf0e-4f5b-be06-e67195b6e3dd
003SwePub
008160401s2003 | |||||||||||000 ||eng|
024a https://lup.lub.lu.se/record/2897742 URI
024a https://doi.org/10.1038/sj.ejhg.52011112 DOI
040 a (SwePub)lu
041 a engb eng
042 9 SwePub
072 7a art2 swepub-publicationtype
072 7a ref2 swepub-contenttype
100a Godard, B4 aut
2451 0a Provision of genetic services in Europe: current practices and issues
264 c 2004-01-13
264 1b Springer Science and Business Media LLC,c 2003
520 a This paper examines the professional and scientific views on the social, ethical and legal issues that impact on the provision of genetic services in Europe. Many aspects have been considered, such as the definition and the aims of genetic services, their organization, the quality assessment, public education, as well as the partnership with patients support groups and the multicultural aspects. The methods was primarily the analysis of professional guidelines, legal frameworks and other documents related to the organization of genetic services, mainly from Europe, but also from USA and international organizations. Then, the method was to examine the background data emerging from an updated report produced by the Concerted Action on Genetic Services in Europe, as well as the issues debated by 43 experts from 17 European countries invited to an international workshop organized by the European Society of Human Genetics Public and Professional Policy Committee in Helsinki, Finland, 8 and 9 September 2000. Some conclusions were identified from the ESHG workshop to arrive at outlines for optimal genetic services. Participants were concerned about equal accessibility and effectiveness of clinical genetic services, quality assessment of services, professional education, multidisciplinarity and division of tasks as well as networking. Within European countries, adherance to the organizational principles of prioritization, regionalization and integration into related health services would maximize equal accessibility and effectiveness of genetic actions. There is a need for harmonization of the rules involved in financial coverage of DNA tests in order to make these available to all Europeans. Clear guidelines for the best practice will ensure that the provision of genetic services develops in a way that is beneficial to its customers, be they health professionals or the public, especially since the coordination of clinical, laboratory and research perspectives within a single organizational structure permits a degree of coherence not often found in other specialties.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Medicinska och farmaceutiska grundvetenskaperx Medicinsk genetik0 (SwePub)301072 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Basic Medicinex Medical Genetics0 (SwePub)301072 hsv//eng
653 a quality control
653 a genetic testing
653 a genetic services
653 a counselling
653 a genetic counselling
653 a Europe
700a Kaariainen, H4 aut
700a Kristoffersson, Ulfu Lund University,Lunds universitet,Avdelningen för klinisk genetik,Institutionen för laboratoriemedicin,Medicinska fakulteten,Division of Clinical Genetics,Department of Laboratory Medicine,Faculty of Medicine4 aut0 (Swepub:lu)kgen-ukr
700a Tranebjaerg, L4 aut
700a Coviello, D4 aut
700a Ayme, S4 aut
710a Avdelningen för klinisk genetikb Institutionen för laboratoriemedicin4 org
773t European Journal of Human Geneticsd : Springer Science and Business Media LLCg 11, s. 13-48q 11<13-48x 1476-5438x 1018-4813
856u http://dx.doi.org/10.1038/sj.ejhg.5201111x freey FULLTEXT
856u https://www.nature.com/articles/5201111.pdf
8564 8u https://lup.lub.lu.se/record/289774
8564 8u https://doi.org/10.1038/sj.ejhg.5201111

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