Combined use of karyotyping and copy number variation sequencing technology in prenatal diagnosis
Background Karyotyping and genome copy number variation sequencing (CNV-seq) are two techniques frequently used in prenatal diagnosis. This study aimed to explore the diagnostic potential of using a combination of these two methods in order to provide a more accurate clinical basis for prenatal diag...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , , , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
PeerJ Inc.
2022-12-01
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| Σειρά: | PeerJ |
| Θέματα: | |
| Διαθέσιμο Online: | https://peerj.com/articles/14400.pdf |
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