Estimate of genetic variants using CNV‐Seq for fetuses with oligohydramnios or polyhydramnios
Abstract Background Oligohydramnios or polyhydramnios, is associated with chromosomal aberrations, particularly aneuploidy. However, its correlation with copy number variation (CNV) remains unclear. Methods We retrospectively analyzed 428 cases with an abnormal level of amniotic fluid, comprising of...
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| Hlavní autoři: | , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Wiley
2023-01-01
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| Edice: | Molecular Genetics & Genomic Medicine |
| Témata: | |
| On-line přístup: | https://doi.org/10.1002/mgg3.2089 |
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