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Shallow whole genome sequencing is well suited for the detection of chromosomal aberrations in human blastocysts.
Deleye L, Dheedene A, De Coninck D, Sante T, Christodoulou C, Heindryckx B, Van den Abbeel E, De Sutter P, Deforce D, Menten B, Van Nieuwerburgh F. Deleye L, et al. Among authors: van den abbeel e, van nieuwerburgh f. Fertil Steril. 2015 Nov;104(5):1276-85.e1. doi: 10.1016/j.fertnstert.2015.07.1144. Epub 2015 Aug 14. Fertil Steril. 2015. PMID: 26282994 Free article.
Whole genome amplification with SurePlex results in better copy number alteration detection using sequencing data compared to the MALBAC method.
Deleye L, De Coninck D, Christodoulou C, Sante T, Dheedene A, Heindryckx B, Van den Abbeel E, De Sutter P, Menten B, Deforce D, Van Nieuwerburgh F. Deleye L, et al. Among authors: van den abbeel e, van nieuwerburgh f. Sci Rep. 2015 Jun 30;5:11711. doi: 10.1038/srep11711. Sci Rep. 2015. PMID: 26122179 Free PMC article.
Preimplantation genetic diagnosis for chromosomal rearrangements with the use of array comparative genomic hybridization at the blastocyst stage.
Christodoulou C, Dheedene A, Heindryckx B, van Nieuwerburgh F, Deforce D, De Sutter P, Menten B, Van den Abbeel E. Christodoulou C, et al. Among authors: van den abbeel e, van nieuwerburgh f. Fertil Steril. 2017 Jan;107(1):212-219.e3. doi: 10.1016/j.fertnstert.2016.09.045. Epub 2016 Oct 25. Fertil Steril. 2017. PMID: 27793373 Free article.
Mutation-free baby born from a mitochondrial encephalopathy, lactic acidosis and stroke-like syndrome carrier after blastocyst trophectoderm preimplantation genetic diagnosis.
Heindryckx B, Neupane J, Vandewoestyne M, Christodoulou C, Jackers Y, Gerris J, Van den Abbeel E, Van Coster R, Deforce D, De Sutter P. Heindryckx B, et al. Among authors: van den abbeel e, van coster r. Mitochondrion. 2014 Sep;18:12-7. doi: 10.1016/j.mito.2014.08.005. Epub 2014 Aug 23. Mitochondrion. 2014. PMID: 25159128
83 results