<p>The present disclosure describes methods for screening and identifying genomic sequences useful in estimating the risk of fetal aneuploidy, particularly trisomy 21. This disclosure also describes methods for utilizing such genomic sequences alone or to augment existing non-invasive diagnostics for Trisomy 21 and other aneuploidies.</p>
申请公布号
WO2007112418(A2)
申请公布日期
2007.10.04
申请号
WO2007US65295
申请日期
2007.03.27
申请人
BAYLOR COLLEGE OF MEDICINE;BISCHOFF, FARIDEH, Z.;SIMPSON, JOE, LEIGH