Enhanced genetic diagnosis in early pregnancy loss: an integrated approach using CNV-Seq and STR genotyping
Abstract Purpose Chromosomal abnormalities are a leading cause of early pregnancy loss (EPL). While copy number variation sequencing (CNV-seq) is gradually applied in clinical practice, its sensitivity for detecting triploidy and uniparental disomy (UPD) remains limited. This study aimed to evaluate...
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| Asıl Yazarlar: | , , , , , , , , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
BMC
2026-05-01
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| Seri Bilgileri: | Reproductive Biology and Endocrinology |
| Konular: | |
| Online Erişim: | https://doi.org/10.1186/s12958-026-01570-9 |
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