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Opening Pandora's box?: ethical issues in prenatal whole genome and exome sequencing
OBJECTIVE: The development of genomic approaches to prenatal testing such as whole genome and exome sequencing offers the potential for a better understanding of prenatal structural anomalies in the fetus and ultimately for improved patient care and more informed reproductive decision making. In add...
Uloženo v:
| Vydáno v: | Prenat Diagn |
|---|---|
| Hlavní autoři: | , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
John Wiley and Sons Inc.
2017
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5836985/ https://ncbi.nlm.nih.gov/pubmed/28695688 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/pd.5114 |
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