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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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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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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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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Karyomapping: a Universal Method for Genome Wide Analysis of Genetic Disease based on Mapping Crossovers between Parental Haplotypes von Handyside, Alan H, Harton, Gary L, Mariani, Brian, Thornhill, Alan R, Affara, Nabeel A, Shaw, Marie-Anne, Griffin, Darren K

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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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DNA-based X-enriched sperm separation as an adjunct to preimplantation genetic testing for the prevention of X-linked disease von LEVINSON, G, KEYVANFAR, K, CALVO, L, SHERINS, R. J, BICK, D, SCHULMAN, J. D, BLACK, S. H, WU, J. C, FUGGER, E. F, FIELDS, R. A, HARTON, G. L, PALMER, F. T, SISSON, M. E, STARR, K. M, DENNISON-LAGOS, L

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Non-disclosing preimplantation genetic diagnosis for Huntington disease von Stern, Harvey J., Harton, Gary L., Sisson, Michael E., Jones, Shirley L., Fallon, Lee A., Thorsell, Lilli P., Getlinger, Michael E., Black, Susan H., Schulman, Joseph 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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染色体异常与男性不育 von Gary L Harton Helen G Tempest

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Nucleated erythrocytes in maternal blood: quantity and quality of fetal cells in enriched populations von Reading, J P, Huffman, J L, Wu, J C, Palmer, F T, Harton, G L, Sisson, M E, Keyvanfar, K, Gresinger, T H, Cochrane, W J, Fallon, L A

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Improved sizing of fragile X CCG repeats by nested polymerase chain reaction von Levinson, Gene, Maddalena, Anne, Palmer, Frances T., Harton, Gary L., Bick, David P., Howard-Peebles, Patricia N., Black, Susan H., Schulman, Joseph D.

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Diagnosing and preventing inherited disease: Nucleated erythrocytes in maternal blood: quantity and quality of fetal cells in enriched populations von Reading, Julian P., Huffman, John L., Wu, Joy C., Palmer, Frances T., Harton, Gary L., E.Sisson, Michael, Keyvanfar, Keyvan, Gresinger, Thomas H., Cochrane, William J., Fallon, Lee A., Menapace-Drew, Gianna F., Cummings, Emilie A., Jones, Shirley L., Black, Susan H., Schulman, Joseph D., Levinson, Gene

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Novel approach to the molecular diagnosis of Marfan syndrome: Application to sporadic cases and in prenatal diagnosis von Toudjarska, Iva, Kilpatrick, Michael W., Lembessis, Peter, Carra, Scott, Harton, Gary L., Sisson, Michael E., Black, Susan H., Stern, Harvey J., Gelman-Kohan, Zully, Shohat, Mordechai, Tsipouras, Petros

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Nucleated erythrocytes in maternal blood : quantity and quality of fetal cell in enriched populations von READING, J. P, HUFFMAN, J. L, MENAPACE-DREW, G. F, CUMMINGS, E. A, JONES, S. L, BLACK, S. H, SCHULMAN, J. D, LEVINSON, G, WU, J. C, PALMER, F. T, HARTON, G. L, SISSON, M. E, KEYVANFAR, K, GRESINGER, T. H, COCHRANE, W. J, FALLON, L. A

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Improved sizing of fragile X CGG repeats by nested polymerase chain reaction: X-linked mental retardation von LEVINSON, G, MADDALENA, A, PALMER, F. T, HARTON, G. L, BICK, D. P, HOWARD-PEEBLES, P. N, BLACK, S. H, SCHULMAN, J. D

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PGDIS Position Statement on the Transfer of Mosaic Embryos 2019 von Cram, D.S., Leigh, D., Handyside, A., Rechitsky, L., Xu, K., Harton, G., Grifo, J., Rubio, C., Fragouli, E., Kahraman, S., Forman, E., Katz-Jaffe, M., Tempest, H., Thornhill, A., Strom, C., Escudero, T., Qiao, J., Munne, S., Simpson, J.L., Kuliev, A.

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Directional light-WIMP time-projection-chamber detector for electron beam-dump experiments von Snowden-Ifft, D. P., Harton, J. L., Ma, Nan, Schuckman, F. G.

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Low threshold results and limits from the DRIFT directional dark matter detector von Battat, J.B.R., Ezeribe, A.C., Gauvreau, J.-L., Harton, J.L., Lafler, R., Law, E., Lee, E.R., Loomba, D., Lumnah, A., Miller, E.H., Monte, A., Mouton, F., Paling, S.M., Phan, N.S., Robinson, M., Sadler, S.W., Scarff, A., Schuckman II, F.G., Snowden-Ifft, D.P., Spooner, N.J.C., Waldram, N.

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