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Low Unconguted Estriol Levels in the Maternal Quadruple-Marker Screen in a Fetus with Cornelia de Lange Syndrome and a Partial Deletion of the NIPBL Gene
by Patrick L. Wilson, Jean Ricci Goodman, Erica Cole, John J. Mulvihill, Ji-Yun Lee, Shibo Li and Andrew Wagner
American Journal of Biomedical Research. 2013, 1(2), 25-27. DOI: 10.12691/ajbr-1-2-1
Pub. Date: March 22, 2013Views: 14324Downloads: 7784
Cornelia de Lange Syndrome prenatal quadruple screen trisomy 18 microarray Smith Lemli Opitz syndrome placenta
Abstract Full Text PDF (246 KB) Full Text HTML Full Text ePUB (165 KB)
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