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Non-invasive epigenetic detection of fetal trisomy 21 in first trimester maternal plasma.
BACKGROUND: Down syndrome (DS) is the most common known aneuploidy, caused by an extra copy of all or part of chromosome 21. Fetal-specific epigenetic markers have been investigated for non-invasive prenatal detection of fetal DS. The phosphodiesterases gene, PDE9A, located on chromosome 21q22.3, is...
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Huvudupphovsmän: | , , , , , , , , , , |
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Materialtyp: | Artigo |
Språk: | Inglês |
Publicerad: |
Public Library of Science (PLoS)
2011-01-01
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Serie: | PLoS ONE |
Länkar: | http://europepmc.org/articles/PMC3223183?pdf=render |
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