Amniotic fluid transcriptomics reflects novel disease mechanisms in fetuses with myelomeningocele. Homo sapiens
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下载链接：
https://www.ncbi.nlm.nih.gov/bioproject/PRJNA393797
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资源简介：
To identify molecular pathophysiologic changes and novel disease mechanisms specific to myelomeningocele by analyzing AFS cfRNA in fetuses with open myelomeningocele. Overall design: AFS was collected from 10 pregnant women at the time of the open myelomeningocele repair in the second trimester (24.5+/-1.0 wks) and 10 archived AFS from sex and gestational age-matched euploid fetuses without myelomeningocele were used as controls (20.9+/-0.9 wks). Differentially regulated gene expression patterns were analyzed using Human Genome U133 Plus 2.0 arrays.
创建时间：
2017-07-11
