CHRISTODOULOS CHRISTODOULOU
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Chromosomal mosaicism in human blastocysts : the ultimate challenge of preimplantation genetic testing?
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Comprehensive comparison of inner cell mass and trophectoderm reveals the complex nature of chromosomal mosaicism in human embryos
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Preimplantation genetic diagnosis for chromosomal rearrangements with the use of array comparative genomic hybridization at the blastocyst stage
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Preimplantation genetic diagnosis (PGD) for translocation carriers using whole genome screening by microarray analysis at the blastocyst stage
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Shallow whole genome sequencing is well suited for the detection of chromosomal aberrations in human blastocysts
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- Journal Article
- A1
- open access
Whole genome amplification with SurePlex results in better copy number alteration detection using sequencing data compared to the MALBAC method
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Mutation-free baby born from a mitochondrial encephalopathy, lactic acidosis and stroke-like syndrome carrier after blastocyst trophectoderm preimplantation genetic diagnosis
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Mutation-free baby born from a mitochondrial encephalopathy, lactic acidosis and stroke-like episodes carrier after trophectoderm pre-implantation genetic diagnosis