Quality in genetic counselling for presymptomatic testing--clinical guidelines for practice across the range of genetic conditions.
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Recommendations for presymptomatic genetic testing and management of individuals at risk for hereditary transthyretin amyloidosisPresymptomatic genetic analysis during pregnancy for vascular type Ehlers-Danlos syndrome.Translating personalized medicine using new genetic technologies in clinical practice: the ethical issuesSCA2 predictive testing in Cuba: challenging concepts and protocol evolution.Quality issues concerning genetic counselling for presymptomatic testing: a European Delphi studyManagement of asymptomatic gene carriers of transthyretin familial amyloid polyneuropathyCancer risk communication, predictive testing and management in France, Germany, the Netherlands and the UK: general practitioners' and breast surgeons' current practice and preferred practice responsibilitiesPresymptomatic ALS genetic counseling and testing: Experience and recommendations.A53T in a parkinsonian family: a clinical update of the SNCA phenotypes.Non-invasive Prenatal Diagnosis for BRCA Mutations - a Qualitative Pilot Study of Health Professionals' Views.Amyotrophic lateral sclerosis in a patient with a family history of huntington disease: genetic counseling challenges.Guidance for patients considering direct-to-consumer genetic testing and health professionals involved in their care: development of a practical decision tool.Predictive genetic testing for amyotrophic lateral sclerosis and frontotemporal dementia: genetic counselling considerations.The Cuban program for predictive testing of SCA2: 11 years and 768 individuals to learn from.Online genetic counseling from the providers' perspective: counselors' evaluations and a time and cost analysis.What counts as effective genetic counselling for presymptomatic testing in late-onset disorders? A study of the consultand's perspective.Mid- and long-term anxiety levels associated with presymptomatic testing of Huntington's disease, Machado-Joseph disease, and familial amyloid polyneuropathy.Case report: concurrent Wilson disease and Huntington disease: lightning can strike twice.Patient and family trajectories of mitochondrial disease: diversity, uncertainty and genetic risk.Genetics 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.Discussions about predictive genetic testing for Lynch syndrome: the role of health professionals and families in decisions to decline.Patient-centered decision making in amyotrophic lateral sclerosis: where are we?Non-invasive prenatal screening for trisomy 21: Consumers' perspectives
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P2860
Quality in genetic counselling for presymptomatic testing--clinical guidelines for practice across the range of genetic conditions.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
Quality in genetic counselling ...... e range of genetic conditions.
@en
Quality in genetic counselling ...... e range of genetic conditions.
@nl
type
label
Quality in genetic counselling ...... e range of genetic conditions.
@en
Quality in genetic counselling ...... e range of genetic conditions.
@nl
prefLabel
Quality in genetic counselling ...... e range of genetic conditions.
@en
Quality in genetic counselling ...... e range of genetic conditions.
@nl
P2860
P356
P1476
Quality in genetic counselling ...... e range of genetic conditions.
@en
P2093
Leigh Jackson
Lesley Goldsmith
P2860
P2888
P304
P356
10.1038/EJHG.2012.174
P577
2012-08-15T00:00:00Z
P6179
1002104520