| scholarly article | Q13442814 |
| P50 | author | Bartha Knoppers | Q2885924 |
| P2860 | cites work | Genomics really gets personal: how exome and whole genome sequencing challenge the ethical framework of human genetics research | Q28601377 |
| ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing | Q29616235 | ||
| Managing incidental findings and research results in genomic research involving biobanks and archived data sets | Q34205284 | ||
| Antenatal genetic testing and the right to remain in ignorance | Q34504632 | ||
| Population studies: return of research results and incidental findings Policy Statement | Q39588665 | ||
| The need to know--therapeutic privilege: a way forward | Q44297306 | ||
| Whole-genome sequencing and the physician | Q48470406 | ||
| P433 | issue | 1 | |
| P304 | page(s) | 6-10 | |
| P577 | publication date | 2014-03-01 | |
| P1433 | published in | Journal of Law, Medicine, and Ethics | Q15760852 |
| P1476 | title | INTRODUCTION: From the Right to Know to the Right Not to Know | |
| P478 | volume | 42 |
| Q92759491 | A RaDiCAL gene hunt |
| Q35772195 | Disclosure of research results in genetic studies of Parkinson's disease caused by LRRK2 mutations |
| Q46030255 | Distinctions in Disclosure: Mandated Informed Consent in Abortion and ART. |
| Q89449985 | Ethical values supporting the disclosure of incidental and secondary findings in clinical genomic testing: a qualitative study |
| Q38947409 | Next-Generation Sequencing and the Return of Results |
| Q38846678 | Prenatal Testing for Adult-Onset Conditions: the Position of the National Society of Genetic Counselors |
| Q47558303 | The Ethics of General Population Preventive Genomic Sequencing: Rights and Social Justice |
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