File:Aneuploidy model based on fragmentation 1.jpg
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Embryonic development was monitored by time-lapse imaging from the one- to four-cell stage followed by assessment of chromosomal composition of each blastomere in the imaged embryos. We observed refinement of diagnostic non-invasive cell cycle parameters, determined the correlation with meiotic (monosomies and trisomies) and mitotic (high and low mosaic) errors and demonstrated an association between the cell cycle parameters and embryo morphology (fragmentation and blastomere asymmetry). We also suggest clinical value of parameter analysis with and without automated fragmentation assessment.
Above text from figure legend and Supplementary refers to the original article supplementary information.
- Links: Abnormal Development - Genetic | Trisomy 21 | Zygote | Morula
Reference
<pubmed>23212380</pubmed>| Nat Commun.
Copyright
http://creativecommons.org/licenses/by-nc-sa/3.0/
Figure 7. Ncomms2249-f7.jpg Original figure altered in size and labelling.
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