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Detection of chromosomal abnormalities in spontaneous miscarriage by low-coverage next-generation sequencing
Chromosomal abnormalities (CAs) can cause spontaneous miscarriage and increase the incidence of subsequent pregnancy loss and other complications. Presently, CAs are detected mainly by array comparative genomic hybridization (CGH) and single nucleotide polymorphism microarrays. The present study dev...
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| Publicado no: | Mol Med Rep |
|---|---|
| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
D.A. Spandidos
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7339674/ https://ncbi.nlm.nih.gov/pubmed/32626971 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/mmr.2020.11208 |
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