ESHRE PGD Consortium data collection V: Cycles from January to December 2002 with pregnancy follow-up to October 2003 von Harper, J.C., Boelaert, K., Geraedts, J., Harton, G., Kearns, W.G., Moutou, C., Muntjewerff, N., Repping, S., SenGupta, S., Scriven, P.N., Traeger-Synodinos, J., Vesela, K., Wilton, L., Sermon, K.D.

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Detection of aneuploidy for chromosomes 4, 6, 7, 8, 9, 10, 11, 12, 13, 17, 18, 21, X and Y by fluorescence in-situ hybridization in spermatozoa from nine patients with oligoastheno... von Pang, M.G., Hoegerman, S.F., Cuticchia, A.J., Moon, S.Y., Doncel, G.F., Acosta, A.A., Kearns, W.G.

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Latent Adeno-Associated Virus Infection Elicits Humoral but Not Cell-Mediated Immune Responses in a Nonhuman Primate Model von Hernandez, Y J, Wang, J, Kearns, W G, Loiler, S, Poirier, A, Flotte, T R

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Aneuploidy frequencies in semen fractions from ten oligoasthenoteratozoospermic patients donating sperm for intracytoplasmic sperm injection von Pfeffer, Jerome, Pang, Myung-Geol, Hoegerman, Stanton F, Osgood, Christopher J, Stacey, M.W, Mayer, Jacob, Oehninger, Sergio, Kearns, William G

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In vivo model of adeno-associated virus vector persistence and rescue von Afione, S A, Conrad, C K, Kearns, W G, Chunduru, S, Adams, R, Reynolds, T C, Guggino, W B, Cutting, G R, Carter, B J, Flotte, T R

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Comprehensive microarray SNP genetic analyses on single cells from polar bodies and embryos to determine and identify source of 23-chromosome aneuploidy and structural chromosome a... von Kearns, WG, Pen, R, Benner, A, Siegel, A, Widra, E, Leach, R

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Introduction and expression of the 400 kilobase precursor amyloid protein gene in transgenic mice von Lamb, Bruce T, Sisodia, Sangram S, Lawler, Ann M, Slunt, Hilda H, Kitt, Cheryl A, Kearns, William G, Pearson, Peter L, Price, Donald L, Gearhart, John D

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Preimplantation Genetic Diagnosis and Screening von Kearns, W.G., Pen, R., Graham, J., Han, T., Carter, J., Moyer, M., Richter, K.S., Tucker, M., Hoegerman, S.F., Widra, E.

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Comprehensive microarray genetic analyses on single cells from human embryos von Kearns, WG, Pen, R, Benner, A, Kittai, A, Sagoskin, A, Widra, E, Leach, R

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Lack of site-specific integration of the recombinant adeno-associated virus 2 genomes in human cells von Ponnazhagan, S, Erikson, D, Kearns, W G, Zhou, S Z, Nahreini, P, Wang, X S, Srivastava, A

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Sex chromosome abnormalities after intracytoplasmic sperm injection von Liebaers, I, Hoegerman, StantonF, Govaerts, I, Tesarik, Jan, Bonduelle, M, Van Assche, E, Devroey, P, Van Steirteghem, A, Pang, Myung-Geol, Kearns, WilliamG, Englert, Y, Vamos, E, Rodesch, F, Hervé, C, Moutel, G

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Centrosome amplification and aneuploidy in bone marrow failure patients von Kearns, William G., Yamaguchi, Hiroki, Young, Neal S., Liu, Johnson M.

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Increased risk for aplastic anemia and myelodysplastic syndrome in individuals lacking glutathione S-transferase genes von Sutton, Joanne F., Stacey, Michael, Kearns, William G., Rieg, Thomas S., Young, Neal S., Liu, Johnson M.

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Genomic instability in bone marrow failure syndromes von Kearns, William G., Sutton, Joanne F., Maciejewski, Jaroslaw P., Young, Neal S., Liu, Johnson M.

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Assignment of the Hypoxia-Inducible Factor 1α Gene to a Region of Conserved Synteny on Mouse Chromosome 12 and Human Chromosome 14q von Semenza, G.L., Rue, E.A., Iyer, N.V., Pang, M.G., Kearns, W.G.

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Absence of donor-derived keratinocyte stem cells in skin tissues cultured from patients after mobilized peripheral blood hematopoietic stem cell transplantation von Hematti, Peiman, Sloand, Elaine M, Carvallo, Cristian A, Albert, Michael R, Yee, Carole L, Fuehrer, Monika M, Blancato, Jan K, Kearns, William G, Barrett, John A, Childs, Richard W, Vogel, Jonathan C, Dunbar, Cynthia E

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Expression of the human multidrug resistance and glucocerebrosidase cDNAs from adeno-associated vectors: efficient promoter activity of AAV sequences and in vivo delivery via lipos... von Baudard, M, Flotte, T R, Aran, J M, Thierry, A R, Pastan, I, Pang, M G, Kearns, W G, Gottesman, M M

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Cytogenetics of somatic cells and sperm from a 46,XY/45,X mosaic male with moderate oligoasthenoteratozoospermia von Newberg, Matthew T., Francisco, Robert G., Pang, Myung-Geol, Brugo, Santiago, Doncel, Gustavo F., Acosta, Anibal A., Hoegerman, Stanton F., Kearns, William G.

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A complex chromosomal rearrangement detected prenatally and studied by fluorescence in situ hybridization von BATISTA, D. A. S, TUCK-MULLER, C. M, MARTINEZ, J. E, KEARNS, W. G, PEARSON, P. L, STETTEN, G

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Nuclear receptor co-repressor gene localizes to 17p11.2, a frequently deleted band in malignant disorders von Stacey, Michael W., Wang, Jianxiang, Byrd, Rebecca L., Liu, Johnson M., Kearns, William G.

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