How Should Patients and Providers Interpret the US Food and Drug Administration's Regulatory Language for Direct-to-Consumer Genetic Tests?
| Errataetall: |
CommentIn: J Clin Oncol. 2020 Jan 20;38(3):283-284. - PMID 31751161 |
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| Medienart: |
E-Artikel |
| Erscheinungsjahr: |
2019 |
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| Erschienen: |
2019 |
| Enthalten in: |
Zur Gesamtaufnahme - volume:37 |
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| Enthalten in: |
Journal of clinical oncology : official journal of the American Society of Clinical Oncology - 37(2019), 28 vom: 01. Okt., Seite 2514-2517 |
| Sprache: |
Englisch |
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| Beteiligte Personen: |
Kilbride, Madison K [VerfasserIn] |
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| Links: |
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| Themen: |
Case Reports |
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| Anmerkungen: |
Date Completed 10.06.2020 Date Revised 10.06.2020 published: Print-Electronic CommentIn: J Clin Oncol. 2020 Jan 20;38(3):283-284. - PMID 31751161 Citation Status MEDLINE |
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| doi: |
10.1200/JCO.18.01418 |
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| funding: |
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| Förderinstitution / Projekttitel: |
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| PPN (Katalog-ID): |
NLM297907549 |
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