发明名称 DIAGNOSTIC TEST FOR THE DETECTION OF CHROMOSOMAL ABNORMALITIES IN A FETUS
摘要 <p>A method for the diagnosis of aneuploidy of a chromosome in a fetus is provided using the polymerase chain reaction. The method utilises a multiplex PCR assay comprising a plurality of chromosome-specific short tandem repeat markers. The method can be used to diagnose fetal trisomy and monosomy responsible for disease conditions such as Down Syndrome and Turner Syndrome, respectively. The method can also be used to diagnose the presence of other genetic conditions such as cystic fibrosis.</p>
申请公布号 WO2002068685(A2) 申请公布日期 2002.09.06
申请号 GB2002000839 申请日期 2002.02.26
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