ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing
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Achieving high-sensitivity for clinical applications using augmented exome sequencingMedical implications of technical accuracy in genome sequencingA Balanced Look at the Implications of Genomic (and Other "Omics") Testing for Disease Diagnosis and Clinical CareGenomic knowledge sharing: A review of the ethical and legal issuesWhole Genome Sequencing as a Genetic Test for Autism Spectrum Disorder: From Bench to Bedside and then Back AgainHas the biobank bubble burst? Withstanding the challenges for sustainable biobanking in the digital eraPractical aspects of NGS-based pathways analysis for personalized cancer science and medicineClinical Genetic Testing in GastroenterologyPersonal Genome Sequencing in Ostensibly Healthy Individuals and the PeopleSeq ConsortiumAssessing the Costs and Cost-Effectiveness of Genomic SequencingIncidental Findings with Genomic Testing: Implications for Genetic Counseling PracticePharmGKB summary: succinylcholine pathway, pharmacokinetics/pharmacodynamicsNext-Generation Sequencing in Clinical Molecular Diagnostics of Cancer: Advantages and ChallengesGenetic studies of quantitative MCI and AD phenotypes in ADNI: Progress, opportunities, and plansNext-generation sequencing to guide cancer therapyClinical application of next-generation sequencing for Mendelian diseasesComparison of delivery strategies for pharmacogenetic testing servicesThe Human Genome Project, and recent advances in personalized genomicsNavigating the rapids: the development of regulated next-generation sequencing-based clinical trial assays and companion diagnosticsBiobanks and personalized medicineGenetic epidemiology and nonsyndromic structural birth defects: from candidate genes to epigeneticsRecommendations for returning genomic incidental findings? We need to talk!Non-invasive prenatal testing: a review of international implementation and challengesCommunicating results in post-Belmont era biomonitoring studies: lessons from genetics and neuroimaging researchEvidence synthesis and guideline development in genomic medicine: current status and future prospectsStakeholder engagement: a key component of integrating genomic information into electronic health recordsReflecting on earlier experiences with unsolicited findings: points to consider for next-generation sequencing and informed consent in diagnosticsUse of contemporary genetics in cardiovascular diagnosisClinical tumor sequencing: opportunities and challenges for precision cancer medicine"Is It Worth Knowing?" Focus Group Participants' Perceived Utility of Genomic Preconception Carrier Screening.Attitudes towards the sharing of genetic information with at-risk relatives: results of a quantitative surveyParticipant use and communication of findings from exome sequencing: a mixed-methods study.Public preferences for the return of research results in genetic research: a conjoint analysisIntegrating next-generation sequencing into clinical oncology: strategies, promises and pitfallsThe possibility of clinical sequencing in the management of cancerPharmGKB summary: very important pharmacogene information for RYR1Insights from exome sequencing for endocrine disordersGermline Heterozygous Variants in SEC23B Are Associated with Cowden Syndrome and Enriched in Apparently Sporadic Thyroid CancerRare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosisDeveloping genomic knowledge bases and databases to support clinical management: current perspectives
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ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing
description
2013 nî lūn-bûn
@nan
2013 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
ACMG recommendations for repor ...... al exome and genome sequencing
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ACMG recommendations for repor ...... al exome and genome sequencing
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type
label
ACMG recommendations for repor ...... al exome and genome sequencing
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ACMG recommendations for repor ...... al exome and genome sequencing
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ACMG recommendations for repor ...... al exome and genome sequencing
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ACMG recommendations for repor ...... al exome and genome sequencing
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ACMG recommendations for repor ...... al exome and genome sequencing
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American College of Medical Genetics and Genomics
Amy L McGuire
Bruce R Korf
Christa L Martin
Kelly E Ormond
Leslie G Biesecker
Michael S Watson
Robert C Green
Robert L Nussbaum
Sarah S Kalia
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10.1038/GIM.2013.73
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2013-06-20T00:00:00Z
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1017226766