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Rare chromosomal abnormalities: Can they be identified using conventional first trimester combined screening methods?
OBJECTIVE: To evaluate the performance of first trimester combined screening for the detection of rare chromosomal abnormalities, other than Trisomies 21, 18 or 13 or 45 × . STUDY DESIGN: A database containing 36,254 pregnancies was analyzed. These patients were recruited at 15 US centers and includ...
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| Veröffentlicht in: | Eur J Obstet Gynecol Reprod Biol X |
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| Hauptverfasser: | , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Elsevier
2021
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7937980/ https://ncbi.nlm.nih.gov/pubmed/33733087 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.eurox.2021.100123 |
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