Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
3274032 | Journal de Gynécologie Obstétrique et Biologie de la Reproduction | 2006 | 7 Pages |
Abstract
. A conventional hemi nested PCR analysis of maternal plasma could be used for accurate fetal RhD status. However this procedure is difficult to apply for routine analysis because of the importance of anti-contamination measures required to obtain good results. Real time quantitative PCR analysis on fetal DNA is more suitable. Whatever the operating procedure used, polymorphism of RhD gene may follow in either false negative from presence of rearranged gene or false positive from occasional presence of a non functional RHD gene.
Keywords
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Authors
D. Dif-Couvreux, V. Houfflin-Debarge, A. Delsalle, S. Dourieux, S. Dubreucq, L. Manessier, F. Puech,