Clinical activity of ponatinib in a patient with FGFR1-rearranged mixed-phenotype acute leukemia von Khodadoust, M S, Luo, B, Medeiros, B C, Johnson, R C, Ewalt, M D, Schalkwyk, A S, Bangs, C D, Cherry, A M, Arai, S, Arber, D A, Zehnder, J L, Gotlib, J

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Human Endothelial Cell Life Extension by Telomerase Expression von Yang, Jiwei, Chang, Edwin, Cherry, Athena M., Bangs, Charles D., Oei, Yoko, Bodnar, Andrea, Bronstein, Adrienne, Chiu, Choy-Pik, Herron, G. Scott

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Natural killer cell precursor acute lymphoma/leukemia presenting in an infant von Natkunam, Y, Cherry, A M, Cornbleet, P J

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Compound genetic factors as a cause of male infertility von BLACK, L. D, NUDELL, D. M, CHA, I, CHERRY, A. M, TUREK, P. J

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Complex or monosomal karyotype and not blast percentage is associated with poor survival in acute myeloid leukemia and myelodysplastic syndrome patients with inv(3)(q21q26.2)/t(3;3... von Rogers, Heesun J, Vardiman, James W, Anastasi, John, Raca, Gordana, Savage, Natasha M, Cherry, Athena M, Arber, Daniel, Moore, Erika, Morrissette, Jennifer J D, Bagg, Adam, Liu, Yen-Chun, Mathew, Susan, Orazi, Attilio, Lin, Pei, Wang, Sa A, Bueso-Ramos, Carlos E, Foucar, Kathryn, Hasserjian, Robert P, Tiu, Ramon V, Karafa, Matthew, Hsi, Eric D

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302 DUPLICATION 22Q11.2: CLINICALLY HETEROGENEOUS NEW SYNDROME OR GENETIC POLYMORPHISM? von Bernstein, J. A., Chen, K. C., Saal, H. M., Alkuraya, F. S., Stevens, C. A., Cherry, A. M., Hoyme, H. E.

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CTCF Mediates Interchromosomal Colocalization between Igf2/H19 and Wsb1/Nf1 von Ling, Jian Qun, Li, Tao, Hu, Ji Fan, Vu, Thanh H., Chen, Hui Ling, Qiu, Xin Wen, Cherry, Athena M., Hoffman, Andrew R.

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339 NABLUS MASK-LIKE FACIAL SYNDROME IS CAUSED BY DELETION IN 8q21-8q22 DETECTED BY ARRAY-BASED COMPARATIVE GENOMIC HYBRIDIZTION von Shieh, J. T.C., Aradhya, S., Manning, M. A., Cherry, A. M., Dallapiccola, B., Hoyme, H. E.

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Array-based comparative genomic hybridization: clinical contexts for targeted and whole-genome designs von Aradhya, Swaroop, Cherry, Athena M

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Preferential expression of a mutant allele of the amplified MDR1 (ABCB1) gene in drug-resistant variants of a human sarcoma von Chen, G. Kevin, Lacayo, Norman J., Durán, George E., Wang, Yan, Bangs, C. Dana, Rea, Susan, Kovacs, Mary, Cherry, Athena M., Brown, J. Martin, Sikic, Branimir I.

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Comprehensive whole-genome sequencing of an early-stage primary myelofibrosis patient defines low mutational burden and non-recurrent candidate genes von Merker, Jason D, Roskin, Krishna M, Ng, Dana, Pan, Cuiping, Fisk, Dianna G, King, Jasmine J, Hoh, Ramona, Stadler, Michael, Okumoto, Lawrence M, Abidi, Parveen, Hewitt, Rhonda, Jones, Carol D, Gojenola, Linda, Clark, Michael J, Zhang, Bing, Cherry, Athena M, George, Tracy I, Snyder, Michael, Boyd, Scott D, Zehnder, James L, Fire, Andrew Z, Gotlib, Jason

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Risk of progression to myelofibrosis and acute myeloid leukemia in patients with essential thrombocythemia and polycythemia vera with prior malignancy von Cherry, M. A., Pham, H., Kantarjian, H., Cortes, J. E., Pierce, S., Zhou, L., Verstovsek, S.

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Insights from the reanalysis of high-throughput chemical genomics data for Escherichia coli K-12 von Wu, Peter I-Fan, Ross, Curtis, Siegele, Deborah A., Hu, James C.

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Role of topotecan, vinorelbine, thiotepa, and gemcitabine (TVTG) chemotheapy in relapsed/refractory adult acute leukemia: A single-institution retrospective analysis von Srour, S. A., Cherry, M. A., Borders, E., Parekh, H., Holter, J. L., Herman, T. S., Selby, G. B.

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Secondary malignancies in essential thrombocythemia and polycythemia vera: A retrospective analysis of 437 patients from a single institution von Pierce, S., Cherry, M. A., Pham, H., Kantarjian, H., Al-Ameri, A., Cortes, J. E., Zhou, L., Verstovsek, S.

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Terminal 22q deletion syndrome: A newly recognized cause of speech and language disability in the autism spectrum von MANNING, Melanie A, CASSIDY, Suzanne B, CLERICUZIO, Carol, CHERRY, Athena M, SCHWARTZ, Stuart, HUDGINS, Louanne, ENNS, Gregory M, HOYME, H. Eugene

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Serosorting Sexual Partners and Risk for HIV Among Men Who Have Sex with Men von Eaton, Lisa A., MA, Kalichman, Seth C., PhD, Cain, Demetria N., MPH, Cherry, Chauncey, MA, Stearns, Heidi L., BA, Amaral, Christina M., BA, Flanagan, Jody A, Pope, Howard L., BS

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Terminal deletion of 6p results in a recognizable phenotype von Lin, Ruth J., Cherry, Athena M., Chen, Kelly C., Lyons, Michael, Hoyme, H. Eugene, Hudgins, Louanne

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Epstein-Barr virus-associated peripheral T-cell lymphoma and hemophagocytic syndrome arising after liver transplantation: Case report and review of the literature von George, Tracy I., Jeng, Michael, Berquist, William, Cherry, Athena M., Link, Michael P., Arber, Daniel A.

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Comparison of interphase FISH and metaphase cytogenetics to study myelodysplastic syndrome: an Eastern Cooperative Oncology Group (ECOG) study von Cherry, Athena M., Brockman, Stephanie R., Paternoster, Sarah F., Hicks, Gary A., Neuberg, Donna, Higgins, Rodney R., Bennett, John M., Greenberg, Peter L., Miller, Kenneth, Tallman, Martin S., Rowe, Jacob, Dewald, Gordon W.

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