Monosomal karyotype in myelodysplastic syndromes, with or without monosomy 7 or 5, is prognostically worse than an otherwise complex karyotype von Patnaik, M M, Hanson, C A, Hodnefield, J M, Knudson, R, Van Dyke, D L, Tefferi, A

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Longitudinal genome-wide analysis of patients with chronic lymphocytic leukemia reveals complex evolution of clonal architecture at disease progression and at the time of relapse von Braggio, E, Kay, N E, VanWier, S, Tschumper, R C, Smoley, S, Eckel-Passow, J E, Sassoon, T, Barrett, M, Van Dyke, D L, Byrd, J C, Jelinek, D F, Shanafelt, T D, Fonseca, R

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Refined cytogenetic-risk categorization for overall and leukemia-free survival in primary myelofibrosis: a single center study of 433 patients von Caramazza, D, Begna, K H, Gangat, N, Vaidya, R, Siragusa, S, Van Dyke, D L, Hanson, C, Pardanani, A, Tefferi, A

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Leukemia risk models in primary myelofibrosis: an International Working Group study von Tefferi, A, Pardanani, A, Gangat, N, Begna, K H, Hanson, C A, Van Dyke, D L, Caramazza, D, Vannucchi, A M, Morra, E, Cazzola, M, Pereira, A, Cervantes, F, Passamonti, F

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Genomic characterization of high-count MBL cases indicates that early detection of driver mutations and subclonal expansion are predictors of adverse clinical outcome von Barrio, S, Shanafelt, T D, Ojha, J, Chaffee, K G, Secreto, C, Kortüm, K M, Pathangey, S, Van-Dyke, D L, Slager, S L, Fonseca, R, Kay, N E, Braggio, E

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Redefining the risks of prenatally ascertained supernumerary marker chromosomes: a collaborative study von Graf, M D, Christ, L, Mascarello, J T, Mowrey, P, Pettenati, M, Stetten, G, Storto, P, Surti, U, Van Dyke, D L, Vance, G H, Wolff, D, Schwartz, S

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Evidence for a Turner Syndrome Locus or Loci at Xp11.2-p22.1 von Zinn, Andrew R., Tonk, Vijay S., Chen, Zhong, Flejter, Wendy L., Gardner, H. Allen, Guerra, Rudy, Kushner, Harvey, Schwartz, Stuart, Sybert, Virginia P., Van Dyke, Daniel L., Ross, Judith L.

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Molecular definition of breakpoints associated with human Xq isochromosomes : Implications for mechanisms of formation von WOLFF, D. J, MILLER, A. P, VAN DYKE, D. L, SCHWARTZ, S, WILLARD, H. F

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The Spreading of X Inactivation into Autosomal Material of an X;autosome Translocation: Evidence for a Difference between Autosomal and X-Chromosomal DNA von White, Wendy M., Willard, Huntington F., Van Dyke, Daniel L., Wolff, Daynna J.

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Deficient Transcription of XIST from Tiny Ring X Chromosomes in Females with Severe Phenotypes von Migeon, Barbara R., Luo, Shengyuan, Stasiowski, Beth A., Jani, Mihir, Axelman, Joyce, Van Dyke, Daniel L., Weiss, Lester, Jacobs, Patricia A., Yang-Feng, Teresa L., Wiley, John E.

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Characterization of Neo-Centromeres in Marker Chromosomes Lacking Detectable Alpha-satellite DNA von Depinet, Theresa W., Zackowski, Joleen L., Earnshaw, William C., Kaffe, Sara, Sekhon, Gurbax S., Stallard, Richard, Sullivan, Beth A., Vance, Gail H., Van Dyke, Daniel L., Willard, Huntington F., Zinn, Arthur B., Schwartz, Stuart

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Cytogenetic analysis and construction of a BAC contig across a common neocentromeric region from 9p von Satinover, D L, Vance, G H, Van Dyke, D L, Schwartz, S

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Molecular characterization of de novo secondary trisomy 13 von Shaffer, L G, McCaskill, C, Han, J Y, Choo, K H, Cutillo, D M, Donnenfeld, A E, Weiss, L, Van Dyke, D L

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Duplication 6q21q23 in two unrelated patients von Pratt, V.M., Roberson, J.R., Weiss, L., Van Dyke, D.L.

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Clinical significance of Y chromosome loss in hematologic disease von Wiktor, Anne, Rybicki, Benjamin A., Piao, Zhe Si, Shurafa, Muhammad, Barthel, Bernd, Maeda, Koichi, Van Dyke, Daniel L.

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Chromosomal aberrations identified in culture of squamous carcinomas are confirmed by fluorescence in situ hybridisation von Worsham, M J, Wolman, S R, Carey, T E, Zarbo, R J, Benninger, M S, Van Dyke, D L

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Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophy von Bodrug, S E, Roberson, J R, Weiss, L, Ray, P N, Worton, R G, Van Dyke, D L

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The frequency of aneuploidy in cultured lymphocytes is correlated with age and gender but not with reproductive history von NOWINSKI, G. P, VAN DYKE, D. L, TILLEY, B. C, JACOBSEN, G, RAMESH BABU, V, WORSHAM, M. J, WILSON, G. N, WEISS, L

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Laboratory guideline for Turner syndrome von Wolff, Daynna J., Van Dyke, Daniel L., Powell, Cynthia M.

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The impact of maternal serum screening programs for Down syndrome in southeast Michigan, 1988-2003 von Van Dyke, D. L., Ebrahim, S. A., Al Saadi, A. A., Powell, S. A., Zenger-Hain, J. L., Micale, M. A., Wiktor, A. E., Zou, Y. S.

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