P724: A unique presentation of triple X syndrome with four copies of SHOX and additional low-level aneuploidy mosaicism von Spaulding, Joanna, Ammouri, Farah, Nielsen, Shelly, VanDyke, Zephyr, Koerselman, Haley, Zaleski, Dianna, Althof, Pamela, Lulla, Dinesh

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Inherited 14q duplication and 21q deletion: A rare adjacent‐2 segregation in multiple family members von Dave, Bhavana J., Olney, Ann Haskins, Zaleski, Dianna H., Pickering, Diane L., Becker, Troy A., Chipman, Hope E., Sanger, Warren G.

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Rapid aneuploidy screening with fluorescence in-situ hybridisation: is it a sufficiently robust stand-alone test for prenatal diagnosis? von Lim, A S T, Lim, T H, Hess, M M, Kee, S K, Lau, Y Y F, Gilbert, R, Hempel, T E, Anderson, K J, Zaleski, D H, Tien, S L, Chia, P, Subramaniam, R, Tan, H K, Tan, A S A, Sanger, W G

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Rearrangements of Chromosome Band 1p36 in Non-Hodgkin’s Lymphoma von DAVE, B. J, HESS, M. M, PICKERING, D. L, ZALESKI, D. H, PFEIFER, A. L, WEISENBURGER, D. D, ARMITAGE, J. O, SANGER, W. G

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Cryptic duplication and deletion of 9q34.3 arrow right qter in a family with a t(9; 22)(q34.3; p11.2) von Sanger, Travis M, Olney, Ann Haskins, Zaleski, Dianna, Pickering, Diane, Nelson, Marilu, Sanger, Warren G, Dave, Bhavana J

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Cryptic duplication and deletion of 9q34.3 → qter in a family with a t(9;22)(q34.3;p11.2) von Sanger, Travis M., Olney, Ann Haskins, Zaleski, Dianna, Pickering, Diane, Nelson, Marilu, Sanger, Warren G., Dave, Bhavana J.

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Holoprosencephaly associated with an apparent isolated 2q37.1→2q37.3 deletion von Lehman, Norman L., Zaleski, Dianna H., Sanger, Warren G., Adickes, Edward D.

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Inherited 14q duplication and 21q deletion: A rare adjacent-2 segregation in multiple family members von Dave, Bhavana J., Olney, Ann Haskins, Zaleski, Dianna H., Pickering, Diane L., Becker, Troy A., Chipman, Hope E., Sanger, Warren G.

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Cryptic duplication and deletion of 9q34.3 → qter in a family with a t(9;22)(q34.3;p11.2) von Sanger, Travis M., Olney, Ann Haskins, Zaleski, Dianna, Pickering, Diane, Nelson, Marilu, Sanger, Warren G., Dave, Bhavana J.

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Familial inverted duplication 7p von Schaefer, G. Bradley, Novak, Kelli, Steele, David, Buehler, Bruce, Smith, Shelley, Zaleski, Dianna, Pickering, Diane, Nelson, Marilu, Sanger, Warren

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Mutations in transforming growth factor-β receptor type II cause familial thoracic aortic aneurysms and dissections von PANNU, Hariyadarshi, FADULU, Van Tran, SHETE, Sanjay, WILLING, Marcia C, RAMAN, C. S, MILEWICZ, Dianna M, CHANG, Jessica, LAFONT, Andrea, HASHAM, Sumera N, SPARKS, Elizabeth, GIAMPIETRO, Philip F, ZALESKI, Christina, ESTRERA, Anthony L, SAFI, Hazim J

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Dynamics of microRNA expression during mouse prenatal development von Rahmanian, Sorena, Murad, Rabi, Breschi, Alessandra, Zeng, Weihua, Mackiewicz, Mark, Williams, Brian, Davis, Carrie A, Roberts, Brian, Meadows, Sarah, Moore, Dianna, Trout, Diane, Zaleski, Chris, Dobin, Alex, Sei, Lei-Hoon, Drenkow, Jorg, Scavelli, Alex, Gingeras, Thomas R, Wold, Barbara J, Myers, Richard M, Guigó, Roderic, Mortazavi, Ali

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Recombinant human complement component C2 produced in a human cell line restores the classical complement pathway activity in-vitro: an alternative treatment for C2 deficiency dise... von Martini, Paolo G V, Cook, Lynette C, Alderucci, Scott, Norton, Angela W, Lundberg, Dianna M, Fish, Susan M, Langsetmo, Knut, Jönsson, Göran, Lood, Christian, Gullstrand, Birgitta, Zaleski, Kate J, Savioli, Nancy, Lottherand, Jason, Bedard, Charles, Gill, John, Concino, Michael F, Heartlein, Michael W, Truedsson, Lennart, Powell, Jan L, Tzianabos, Arthur O

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