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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Detalles Bibliográficos
Autores principales: Wang, Ming-zhu, Lin, Fang-qin, Li, Min, He, Dan, Yu, Qi-hong, Yang, Xue-xi, Wu, Ying-song
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2017
Materias:
Clinical Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5707912/
https://www.ncbi.nlm.nih.gov/pubmed/29162795
http://dx.doi.org/10.12659/MSM.905094

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5707912/
https://www.ncbi.nlm.nih.gov/pubmed/29162795
http://dx.doi.org/10.12659/MSM.905094

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