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FOXD1 mutations are related to repeated implantation failure, intra-uterine growth restriction and preeclampsia
BACKGROUND: Human reproductive disorders consist of frequently occurring dysfunctions including a broad range of phenotypes affecting fertility and women’s health during pregnancy. Several female-related diseases have been associated with hypofertility/infertility phenotypes, such as recurrent pregn...
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| Veröffentlicht in: | Mol Med |
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| Hauptverfasser: | , , , , , , , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
BioMed Central
2019
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6688323/ https://ncbi.nlm.nih.gov/pubmed/31395028 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s10020-019-0104-3 |
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