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Semiconductor Sequencing Analysis of Chromosomal Copy Number Variations in Spontaneous Miscarriage
BACKGROUND: Array CGH is the criterion standard for identifying copy number variations (CNV), but the restrictive requirement of DNA quality and relatively high cost prevent the use of this method as a general assay in hospitals in developing countries. Our principal objective was to determine wheth...
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| Publicado no: | Med Sci Monit |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
International Scientific Literature, Inc.
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5707912/ https://ncbi.nlm.nih.gov/pubmed/29162795 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12659/MSM.905094 |
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