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Application value of NIPT for uncommon fetal chromosomal abnormalities
Abstract Objective To investigate the clinical value of noninvasive prenatal testing (NIPT) for fetal chromosomal deletion, duplication, and sex chromosome abnormalities. Methods The study included 6239 pregnant women with singletons in the first and second trimester of pregnancy who received NIPT f...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , , , |
|---|---|
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
BMC
2020-08-01
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| Σειρά: | Molecular Cytogenetics |
| Θέματα: | |
| Διαθέσιμο Online: | http://link.springer.com/article/10.1186/s13039-020-00508-z |
| Ετικέτες: |
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