Quality assessment of genetic counseling process in the context of presymptomatic testing for late-onset disorders: a thematic analysis of three review articles

scientific article published on 05 August 2011

Quality assessment of genetic counseling process in the context of presymptomatic testing for late-onset disorders: a thematic analysis of three review articles is …
instance of (P31):
scholarly articleQ13442814
meta-analysisQ815382
review articleQ7318358

External links are
P356DOI10.1089/GTMB.2011.0023
P698PubMed publication ID21819246
P5875ResearchGate publication ID51549767

P50authorHeather SkirtonQ42416963
Jorge SequeirosQ47168189
Milena PanequeQ55208650
P2860cites workConducting a critical interpretive synthesis of the literature on access to healthcare by vulnerable groupsQ33251994
P433issue1
P921main subjectreview articleQ7318358
P304page(s)36-45
P577publication date2011-08-05
P1433published inGenetic Testing and Molecular BiomarkersQ15753742
P1476titleQuality assessment of genetic counseling process in the context of presymptomatic testing for late-onset disorders: a thematic analysis of three review articles
P478volume16

Reverse relations

cites work (P2860)
Q41002513Analysis of the Reasons for Non-Uptake of Predictive Testing for Huntington's Disease in Spain: A Qualitative Study
Q49551487Communication of cancer-related genetic and genomic information: A landscape analysis of reviews
Q59047808Effectiveness of the Interventions Utilized in Genetic Counseling
Q45744248From constraints to opportunities? Provision of psychosocial support in portuguese oncogenetic counseling services
Q39034272Genetic Counseling in Portugal: Education, Practice and a Developing Profession
Q38833267Genetic counseling and testing for Huntington's disease: A historical review
Q47713917Genetics Health Professionals' Views on Quality of Genetic Counseling Service Provision for Presymptomatic Testing in Late-Onset Neurological Diseases in Portugal: Core Components, Specific Challenges and the Need for Assessment Tools
Q53359387Identification and characterization of D410E, a novel mutation in the loop 3 domain of CASR, in autosomal dominant hypocalcemia and a therapeutic approach using a novel calcilytic, AXT914.
Q42237704Quality in genetic counselling for presymptomatic testing--clinical guidelines for practice across the range of genetic conditions
Q36184538Quality issues concerning genetic counselling for presymptomatic testing: a European Delphi study
Q45291281What counts as effective genetic counselling for presymptomatic testing in late-onset disorders? A study of the consultand's perspective.

Search more.