I9 Genome-wide analysis by array CGH and karyomapping for aneuploidy testing by Handyside, A.H

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S10 Cleavage stage and blastocyst biopsy by Handyside, A.H

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C1 Twenty years of designer babies by Handyside, A.H

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Nuclear organization in human sperm: preliminary evidence for altered sex chromosome centromere position in infertile males by Finch, K.A., Fonseka, K.G.L., Abogrein, A., Ioannou, D., Handyside, A.H., Thornhill, A.R., Hickson, N., Griffin, D.K.

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O-5 Karyomapping accurately replicates the outcome of conventional genetic testing in PGD of beta-thalassemia without the need for prior test development by Coskun, S, Qubbaj, W, AlHassan, S, Natesan, S, Handyside, A.H

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S16 Karyomapping as a means of universal diagnosis and providing insight into early human development by Griffin, D.K, Thornhill, A.R, Gordon, A, Handyside, A.H

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O-9 Maternal age and not patient history is the main indication for preimplantation genetic screening for aneuploidy and correlates with morphokinetic time lapse analysis by Davies, S, Christopikou, D, Tsorva, E, Karagianni, T, Handyside, A.H, Mastrominas, M

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O2 Altered morphokinetic parameters of embryos identified as aneuploid by single cell array CGH analysis at the 8-cell stage by Davies, S, Christopikou, D, Tsorva, E, Karagianni, T, Mastrominas, M, Handyside, A.H

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P11 Sperm aneuploidy: When to stop counting? by Tempest, H.G, Gillott, D.J, Grigorova, M, Handyside, A.H, Thornhill, A.R

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P3 24 chromosome PGS: Position not quantity by Ioannou, D, Fonseka, K.G.L, Ellis, M, Meershoek, E, Handyside, A.H, Thornhill, A.R, Griffin, D.K

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Analysis of bovine blastocysts indicates ovarian stimulation does not induce chromosome errors, nor discordance between inner-cell mass and trophectoderm lineages by Tutt, D.A.R., Silvestri, G., Serrano-Albal, M., Simmons, R.J., Kwong, W.Y., Guven-Ates, G., Canedo-Ribeiro, C., Labrecque, R., Blondin, P., Handyside, A.H., Griffin, D.K., Sinclair, K.D.

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Pregnancy following exclusion testing for SCA3 on polar bodies in a fresh cycle: a comparison of STR-based targeted haplotyping and genome-wide SNP analysis and meiomapping by Laitinen-Forsblom, P.J., Poost, B., Noss, D., Handyside, A.H., Nevinny-Stickel-Hinzpeter, C.

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Non-invasive measurement of glucose and pyruvate uptake by individual human oocytes and preimplantation embryos by Hardy, K., Hooper, M.A.K., Handyside, A.H., Rutherford, A.J., Winston, R.M.L., Leese, H.J.

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Controlling misdiagnosis errors in preimplantation genetic diagnosis: a comprehensive model encompassing extrinsic and intrinsic sources of error by Lewis, C.M., Pinêl, T., Whittaker, J.C., Handyside, A.H.

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Lack of cell cycle checkpoints in human cleavage stage embryos revealed by a clonal pattern of chromosomal mosaicism analysed by sequential multicolour FISH by Harrison, R.H., Kuo, H.-C., Scriven, P.N., Handyside, A.H., Ogilvie, C. Mackie

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Spindle abnormalities in normally developing and arrested human preimplantation embryos in vitro identified by confocal laser scanning microscopy by Chatzimeletiou, K., Morrison, E.E., Prapas, N., Prapas, Y., Handyside, A.H.

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Fertilization and early embryology: The zona reaction in human oocytes as seen with scanning electron microscopy by Nikas, G., Paraschos, T., Psychoyos, A., Handyside, A.H.

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Preimplantation genetic diagnosis of β-thalassaemia major by Ray, P.F., Kaeda, J.S., Bingham, J., Roberts, I., Handyside, A.H.

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Fluorescent in-situ hybridization to interphase nuclei of human preimplantation embryos with X and Y chromosome specific probes by Griffin, D.K., Handyside, A.H., Penketh, R.J.A., Winston, R.M.L., Delhanty, J.D.A.

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R-175. Chromosome analysis of human preimplantation embryos from fertile patients by Harper, J.C., Ao, A., Handyside, A.H., Winston, R.M.L., Delhanty, J.D.A.

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