E-MTAB-1725 - Comparative genomic hybridization by array of chorionic villi from foetuses diagnosed as euploid or aneuploid by routine cytogenetic analysis to evaluate the usefulness of the CGH+SNP array in clinical diagnosis
Released on 23 January 2014, last updated on 3 June 2014
Products of conception that were diagnosed either euploid or aneuploid during routine cytogenetic analysis were analysed by a novel CGH+SNP array for the evaluation of its usefulness in clinical diagnostics.
comparative genomic hybridization by array, array platform comparison, clinical history, comparative genome hybridization
Diagnostic utility of novel combined CGH+SNP-Arrays for genome-wide simultaneous detection of aneuploidy and uniparental isodisomy in spontaneous abortions. Stefanie Bug, Beate Solfrank, Felizitas Schmitz, Jana Pricelius, Mona Stecher, Sonja Bingemann, Birgit Becker, Andrew Craig, Marc Botcherby, Claudia Nevinny-Stickel-Hinzpeter.
Diagnostic utility of novel combined arrays for genome-wide simultaneous detection of aneuploidy and uniparental isodisomy in losses of pregnancy. Bug S, Solfrank B, Schmitz F, Pricelius J, Stecher M, Craig A, Botcherby M, Nevinny-Stickel-Hinzpeter C. :43 (2014), Europe PMC 25013457