scholarly article | Q13442814 |
P356 | DOI | 10.1038/S41436-018-0391-Z |
P698 | PubMed publication ID | 30578420 |
P50 | author | David T. Miller | Q91603806 |
P2093 | author name string | Joshua L Deignan | |
Reed E Pyeritz | |||
Jodi D Hoffman | |||
James O'Leary | |||
Robert G Best | |||
Ingrid Holm | |||
David Flannery | |||
ACMG Social Ethical Legal Issues Committee | |||
Karen L David | |||
Leslie Manace Brenman | |||
Lynn Bush | |||
P2860 | cites work | Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium | Q28601251 |
Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology | Q34465792 | ||
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics | Q34544874 | ||
Managing the ethical challenges of next-generation sequencing in genomic medicine | Q38239811 | ||
HIPAA's Individual Right of Access to Genomic Data: Reconciling Safety and Civil Rights | Q47198411 | ||
Duty to re-contact. | Q53492995 | ||
Points to consider in the clinical application of genomic sequencing | Q84730858 | ||
The coming explosion in genetic testing--is there a duty to recontact? | Q85087734 | ||
P433 | issue | 4 | |
P921 | main subject | genomics | Q222046 |
medical genetics | Q1071953 | ||
P304 | page(s) | 769-771 | |
P577 | publication date | 2018-12-22 | |
P1433 | published in | Genetics in Medicine | Q15765508 |
P1476 | title | Patient re-contact after revision of genomic test results: points to consider-a statement of the American College of Medical Genetics and Genomics (ACMG) | |
P478 | volume | 21 |
Q92738841 | A duty to recontact in genetics: context matters |
Q90438987 | A pediatric perspective on genomics and prevention in the twenty-first century |
Q94671482 | CFTR variant testing: a technical standard of the American College of Medical Genetics and Genomics (ACMG) |
Q99402854 | Clinical and psychological outcomes of receiving a variant of uncertain significance from multigene panel testing or genomic sequencing: a systematic review and meta-analysis |
Q90103411 | Preemptively Precise: Returning and Updating Pharmacogenetic Test Results to Realize the Benefits of Preemptive Testing |
Q91731430 | Reanalysis and reclassification of rare genetic variants associated with inherited arrhythmogenic syndromes |
Q93012834 | Response to Knoppers et al |
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