Mann, Kathy <br/><br/>
Quantitative fluorescence PCR analysis of >40,000 prenatal samples for the rapid diagnosis of trisomies 13, 18 and 21 and monosomy X.  [electronic resource] 

 -  Prenatal diagnosis  Dec 2012 
 - 1197-204 p.  digital 
<br/><br/> Publication Type: Evaluation Study; Journal Article 
<br/><br/><label>ISSN: </label>1097-0223 
<br/><br/><label>Standard No.: </label>10.1002/pd.3986  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Chromosomes, Human, Pair 13<br/>Chromosomes, Human, Pair 18<br/>Chromosomes, Human, Pair 21<br/>Chromosomes, Human, X<br/>Female<br/>Fluorescence<br/>Humans<br/>Monosomy--diagnosis<br/>Polymerase Chain Reaction--methods<br/>Pregnancy<br/>Prenatal Diagnosis--methods<br/>Retrospective Studies<br/>Sex Chromosome Aberrations<br/>Time Factors<br/>Trisomy--diagnosis