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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Autores principales: Lim, Ji Hyae, Kim, Shin Young, Park, So Yeon, Lee, Shin Yeong, Kim, Mi Jin, Han, You Jung, Lee, Si Won, Chung, Jin Hoon, Kim, Moon Young, Yang, Jae Hyug, Ryu, Hyun Mee
Formato: Artigo
Lenguaje:Inglês
Publicado: Public Library of Science 2011
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Research Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC3223183/
https://ncbi.nlm.nih.gov/pubmed/22132128
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0027709
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