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To identify molecular pathophysiologic changes and novel disease mechanisms specific to myelomeningocele by analyzing AFS cfRNA in fetuses with open myelomeningocele.
ORGANISM(S): Homo sapiens 
2017-07-12 | GSE101141 | GEO
Genetic variations in human with myelomeningocele
Genomics
Spinal Cord transcriptomics in myelomeningocele (MMC) RA-induced rats
Amniotic fluid transcriptomics reflects novel disease mechanisms in fetuses with myelomeningocele
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