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Noninvasive chromosome screening of human embryos by genome sequencing of embryo culture medium for in vitro fertilization
Preimplantation genetic screening (PGS) is widely used to select in vitro-fertilized embryos free of chromosomal abnormalities and to improve the clinical outcome of in vitro fertilization (IVF). A disadvantage of PGS is that it requires biopsy of the preimplantation human embryo, which can limit th...
Tallennettuna:
| Julkaisussa: | Proc Natl Acad Sci U S A |
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| Päätekijät: | , , , , , , , , , , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
National Academy of Sciences
2016
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5081593/ https://ncbi.nlm.nih.gov/pubmed/27688762 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1613294113 |
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