Genetic testing in asymptomatic minors: Recommendations of the European Society of Human Genetics.
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Familial hypercholesterolaemia is underdiagnosed and undertreated in the general population: guidance for clinicians to prevent coronary heart disease: consensus statement of the European Atherosclerosis SocietyWhole-genome sequencing in health care. Recommendations of the European Society of Human Genetics.Whole-genome sequencing in health care: recommendations of the European Society of Human Genetics.Consulting communities on feedback of genetic findings in international health research: sharing sickle cell disease and carrier information in coastal Kenya.Management of hereditary angioedema in pregnant women: a review.The best interests of the child and the return of results in genetic research: international comparative perspectives.Reconsidering reproductive benefit through newborn screening: a systematic review of guidelines on preconception, prenatal and newborn screening.Consensus and controversies in best practices for molecular genetic testing of spinocerebellar ataxias.Statement of the ESHG on direct-to-consumer genetic testing for health-related purposes.Emerging issues in public health genomics.The 'thousand-dollar genome': an ethical exploration.Direct-to-consumer genetic testing in Slovenia: availability, ethical dilemmas and legislation.Parental attitudes toward ethical and social issues surrounding the expansion of newborn screening using new technologiesPublic support for neonatal screening for Pompe disease, a broad-phenotype condition.Familial hypercholesterolaemia in children and adolescents: gaining decades of life by optimizing detection and treatment.Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening.Feasibility of an Assessment Tool for Children's Competence to Consent to Predictive Genetic Testing: a Pilot Study.Genotype prediction of adult type 2 diabetes from adolescence in a multiracial population.A qualitative study to explore how professionals in the United Kingdom make decisions to test children for a sickle cell carrier status.Intrafamilial disclosure of risk for hereditary breast and ovarian cancer: points to considerGenetic susceptibility testing for neurodegenerative diseases: ethical and practice issues.A review of quality of life after predictive testing for and earlier identification of neurodegenerative diseases.Experience, knowledge, and opinions about childhood genetic testing in Batten disease.Experiences of predictive testing in young people at risk of Huntington's disease, familial cardiomyopathy or hereditary breast and ovarian cancer.Genetic counselling in ALS: facts, uncertainties and clinical suggestions.Managing the ethical challenges of next-generation sequencing in genomic medicine.Genome-Wide Sequencing for Prenatal Detection of Fetal Single-Gene Disorders.Whole-exome sequencing in pediatrics: parents' considerations toward return of unsolicited findings for their child.Ethical issues in pediatric genetic testing and screening.Disparities in current and future childhood and newborn carrier identification.What ethical and legal principles should guide the genotyping of children as part of a personalised screening programme for common cancer?Quality in genetic counselling for presymptomatic testing--clinical guidelines for practice across the range of genetic conditions.Clinicians' attitude towards family planning and timing of diagnosis in autosomal dominant polycystic kidney disease.Premature guidance about whole-genome sequencing.Contemporary genetic testing in inherited cardiac disease: tools, ethical issues, and clinical applications.Predictive Psychiatric Genetic Testing in Minors: An Exploration of the Non-Medical Benefits.Is Autosomal Dominant Polycystic Kidney Disease Becoming a Pediatric Disorder?"Both Sides of the Wheelchair": The Views of Individuals with, and Parents of Individuals with Friedreich Ataxia Regarding Pre-symptomatic Testing of Minors.Is There a Right Time to Know? The Right Not to Know and Genetic Testing in Children.Advances in prenatal screening: the ethical dimension.
P2860
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P2860
Genetic testing in asymptomatic minors: Recommendations of the European Society of Human Genetics.
description
2009 nî lūn-bûn
@nan
2009 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի մարտին հրատարակված գիտական հոդված
@hy
2009年の論文
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2009年論文
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2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
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2009年论文
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name
Genetic testing in asymptomati ...... ean Society of Human Genetics.
@ast
Genetic testing in asymptomati ...... ean Society of Human Genetics.
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Genetic testing in asymptomati ...... ean Society of Human Genetics.
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type
label
Genetic testing in asymptomati ...... ean Society of Human Genetics.
@ast
Genetic testing in asymptomati ...... ean Society of Human Genetics.
@en
Genetic testing in asymptomati ...... ean Society of Human Genetics.
@nl
prefLabel
Genetic testing in asymptomati ...... ean Society of Human Genetics.
@ast
Genetic testing in asymptomati ...... ean Society of Human Genetics.
@en
Genetic testing in asymptomati ...... ean Society of Human Genetics.
@nl
P356
P1476
Genetic testing in asymptomati ...... ean Society of Human Genetics.
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P2093
European Society of Human Genetics
P2888
P304
P356
10.1038/EJHG.2009.26
P577
2009-03-11T00:00:00Z