ESHRE PGD Consortium ‘Best practice guidelines for clinical preimplantation genetic diagnosis (PGD) and preimplantation genetic screening (PGS)’ von Thornhill, A.R., deDie-Smulders, C.E., Geraedts, J.P., Harper, J.C., Harton, G.L., Lavery, S.A., Moutou, C., Robinson, M.D., Schmutzler, A.G., Scriven, P.N., Sermon, K.D., Wilton, L.

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Preconception screening and preimplantation genetic diagnosis (PGD): for what are you really getting tested? von Fischer, J, Munne, S, Harton, G.L

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Genome wide karyomapping for preimplantation genetic diagnosis (PGD) detects inherited chromosomal aneuploidies von Handyside, A.H, Zech, N.H, Mariani, B, Harton, G.L

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The types of chromosome abnormality in blastocysts generated by infertile patients von Harton, G.L, Al-Farawaty, S, Goodall, N.-N, Tormasi, S, Wells, D, Fragouli, E

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ESHRE PGD consortium best practice guidelines for amplification-based PGD von Harton, G.L., De Rycke, M., Fiorentino, F., Moutou, C., SenGupta, S., Traeger-Synodinos, J., Harper, J.C.

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ESHRE PGD Consortium/Embryology Special Interest Group—best practice guidelines for polar body and embryo biopsy for preimplantation genetic diagnosis/screening (PGD/PGS) von Harton, G.L., Magli, M.C., Lundin, K., Montag, M., Lemmen, J., Harper, J.C.

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Recombination mapping: a universal molecular karyotyping method for preimplantation genetic diagnosis of inherited disease von Handyside, A.H, Thornhill, A.R, Affara, N.A, Harton, G.L, Mariani, B.D, Griffin, D.K

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Prediction of a balanced rearrangement by preimplantation genetic screening (PGS) von Snider, A.C., Darvin, T.J., Kayali, R., Cinnioglu, C., Harton, G.L.

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Preimplantation genetic diagnosis of sickle-cell/c β-globin mutations using a single base extension genotyping assay von Mariani, B.D, Meltzer, B.W, Reeves, M.J, Harton, G.L, Stern, H.J

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Embryo mosaicism in PGT-A: clinician preferences in reporting von Joshi, N., Harton, G.L., Kayali, R., Akopians, A.L., Surrey, M., Danzer, H., Barritt, J.

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ESHRE PGD consortium best practice guidelines for fluorescence in situ hybridization-based PGD von Harton, G.L., Harper, J.C., Coonen, E., Pehlivan, T., Vesela, K., Wilton, L.

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Different contribution of maternal and paternal age to mosaicism and partial duplication/deletions in blastocyst biopsies assessed by next generation sequencing von Rodrigo, L., Peinado, V., Vera-Rodriguez, M., Lopez-Iglesias, P., Navarro, R., Harton, G.L., Simon, C., Rubio, C.

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Blastocyst Formation Is Not Highly Predictive of a Normal Chromosomal Status of Preimplantation Embryo von Srivastava, R.K., Harton, G.L., Seabaugh, A., Pabon, J.E.

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Successful Implantation and Ongoing Pregnancy of a Single Monosomy 16 Preimplantation Embryo: Case Report von Pabon, J.E., Harton, G.L., Seabaugh, A., Maitta, R., Srivastava, R.K.

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Preimplantation genetic diagnosis for spinal muscular atrophy type I von FALLON, L, HARTON, G. L, BICK, D, SCHULMAN, J, LEVINSON, G, BLACK, S. H, SISSON, M. E, RODRIGUEZ, E, FIELD, L. K, FUGGER, E. F, GELTINGER, M, SUN, Y, DORFMANN, A, SCHOENER, C

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MicroSort® Separation of X- and Y-chromosome bearing sperm: ongoing clinical trial results after intrauterine insemination (IUI), in-vitro fertilization (IVF), and intracytoplasmic... von Fugger, E.F, Keyvanfar, K, Matken, R, Harton, G.L, Stern, H.J, Blauer, K.L

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Reliable gender screening for human preimplantation embryos, using multiple DNA target-sequences von Levinson, G., Fields, R.A., Harton, G.L., Palmer, F.T., Maddalena, A., Fugger, E.F., Schulman, J.D.

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Preimplantation genetic testing for Marfan syndrome von Harton, G.L., Tsipouras, P., Sisson, M.E., Starr, K.M., Mahoney, B.S., Fugger, E.F., Schulman, J.D., Kilpatrick, M.W., Levinson, G., Black, S.H.

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