Incidental findings from clinical genome-wide sequencing: a review.
about
Stakeholder views on secondary findings in whole-genome and whole-exome sequencing: a systematic review of quantitative and qualitative studies.Genetic counseling in direct-to-consumer exome sequencing: a case report.Translating personalized medicine using new genetic technologies in clinical practice: the ethical issuesReturning incidental findings from genetic research to children: views of parents of children affected by rare diseasesDisease variants in genomes of 44 centenarians.Institutional protocol to manage consanguinity detected by genetic testing in pregnancy in a minorResearch participants in NGS studies want to know about incidental findingsReturning a Research Participant's Genomic Results to Relatives: Analysis and Recommendations.Genomic newborn screening: public health policy considerations and recommendations.Compare and contrast: a cross-national study across UK, USA and Greek experts regarding return of incidental findings from clinical sequencingHow can psychological science inform research about genetic counseling for clinical genomic sequencing?How, who, and when: preferences for delivery of genome sequencing results among women diagnosed with breast cancer at a young age.Defining and managing incidental findings in genetic and genomic practice.Genetics in myeloma: genetic technologies and their application to screening approaches in myeloma.Genome-Wide Sequencing for Prenatal Detection of Fetal Single-Gene Disorders.Expect the unexpected: screening for secondary findings in clinical genomics research."I would like to discuss it further with an expert": a focus group study of Finnish adults' perspectives on genetic secondary findings.Screening and overdiagnosis: public health implications.Genomic information and a person's right not to know: A closer look at variations in hypothetical informational preferences in a German sample.Current controversies in prenatal diagnosis 2: should a fetal exome be used in the assessment of a dysmorphic or malformed fetus?
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P2860
Incidental findings from clinical genome-wide sequencing: a review.
description
article científic
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article scientifique
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articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
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artigo científico
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artikel ilmiah
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artikull shkencor
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artículo científico
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name
Incidental findings from clinical genome-wide sequencing: a review.
@en
type
label
Incidental findings from clinical genome-wide sequencing: a review.
@en
prefLabel
Incidental findings from clinical genome-wide sequencing: a review.
@en
P2093
P2860
P1476
Incidental findings from clinical genome-wide sequencing: a review.
@en
P2093
P2860
P304
P356
10.1007/S10897-013-9604-4
P50
P577
2013-05-26T00:00:00Z