Androgenetic/biparental mosaicism causes placental mesenchymal dysplasia von Kaiser-Rogers, K A, McFadden, D E, Livasy, C A, Dansereau, J, Jiang, R, Knops, J F, Lefebvre, L, Rao, K W, Robinson, W P

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Secondary cytogenetic changes in acute promyelocytic leukemia--prognostic importance in patients treated with chemotherapy alone and association with the intron 3 breakpoint of the... von SLACK, J. L, ARTHUR, D. C, RAO, K. W, SCHIFFER, C. A, BLOOMFIELD, C. D, LAWRENCE, D, MROZEK, K, MAYER, R. J, DAVEY, F. R, TANTRAVAHI, R, PETTENATI, M. J, BIGNER, S, CARROLL, A. J

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Adult patients with de novo acute myeloid leukemia and t(9;11)(p22;q23) have a superior outcome to patients with other translocations involving band 11q23 : A cancer and leukemia g... von MROZEK, K, HEINONEN, K, SCHIFFER, C. A, BLOOMFIELD, C. D, LAWRENCE, D, CARROLL, A. J, KODURU, P. R. K, RAO, K. W, STROUT, M. P, HUTCHISON, R. E, MOORE, J. O, MAYER, R. J

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MATERNAL UNIPARENTAL DISOMY OF CHROMOSOME 2 AND CONFINED PLACENTAL MOSAICISM FOR TRISOMY 2 IN A FETUS WITH INTRAUTERINE GROWTH RESTRICTION, HYPOSPADIAS, AND OLIGOHYDRAMNIOS von HANSEN, WENDY F., BERNARD, LYNN E., LANGLOIS, SYLVIE, RAO, KATHLEEN W., CHESCHEIR, NANCY C., AYLSWORTH, ARTHUR S., SMITH, D. IAN, ROBINSON, WENDY P., BARRETT, IRENE J., KALOUSEK, DAGMAR K.

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Functional Correction of Fanconi Anemia Group A Hematopoietic Cells by Retroviral Gene Transfer von Fu, Kai-Ling, Foe, Jerome R. Lo Ten, Joenje, Hans, Rao, Kathleen W., Liu, Johnson M., Walsh, Christopher E.

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American College of Medical Genetics recommendations for the design and performance expectations for clinical genomic copy number microarrays intended for use in the postnatal sett... von Kearney, Hutton M., South, Sarah T., Wolff, Daynna J., Lamb, Allen, Hamosh, Ada, Rao, Kathleen W.

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Molecular characterisation of chromosome 4p deletions resulting in Wolf-Hirschhorn syndrome von Estabrooks, L L, Lamb, A N, Aylsworth, A S, Callanan, N P, Rao, K W

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Section E9 of the American College of Medical Genetics technical standards and guidelines: Fluorescence in situ hybridization von Mascarello, James T., Hirsch, Betsy, Kearney, Hutton M., Ketterling, Rhett P., Olson, Susan B., Quigley, Denise I., Rao, Kathleen W., Tepperberg, James H., Tsuchiya, Karen D., Wiktor, Anne E.

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Functional Correction of Fanconi Anemia Group C Hematopoietic Cells by the Use of a Novel Lentiviral Vector von Yamada, Kaoru, Olsen, John C., Patel, Manij, Rao, Kathleen W., Walsh, Christopher E.

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Pretreatment cytogenetic abnormalities are predictive of induction success, cumulative incidence of relapse, and overall survival in adult patients with de novo acute myeloid leuke... von Byrd, John C., Mrózek, Krzysztof, Dodge, Richard K., Carroll, Andrew J., Edwards, Colin G., Arthur, Diane C., Pettenati, Mark J., Patil, Shivanand R., Rao, Kathleen W., Watson, Michael S., Koduru, Prasad R.K., Moore, Joseph O., Stone, Richard M., Mayer, Robert J., Feldman, Eric J., Davey, Frederick R., Schiffer, Charles A., Larson, Richard A., Bloomfield, Clara D.

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Central review of cytogenetics is necessary for cooperative group correlative and clinical studies of adult acute leukemia : The Cancer and Leukemia Group B experience von FMROZEK, Krzyszto, CARROLL, Andrew J, KODURU, Prasad R. K, BLOCK, Annemarie W, QUMSIYEH, Mazin B, EDWARDS, Colin G, STERLING, Lisa J, HOLLAND, Kelsi B, BLOOMFIELD, Clara D, MAHARRY, Kati, RAO, Kathleen W, PATIL, Shivanand R, PETTENATI, Mark J, WATSON, Michael S, ARTHUR, Diane C, TANTRAVAHI, Ramana, HEEREMA, Nyla A

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Monozygotic twins discordant for partial trisomy 1 von Watson, William J., Katz, Vern L., Albright, Susan G., Rao, Kathleen W., Aylsworth, Arthur S.

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Submicroscopic deletion 9(q34.4) and duplication 19(p13.3): Identified by subtelomere specific FISH probes von Quigley, Denise I., Kaiser‐Rogers, Kathleen, Aylsworth, Arthur S., Rao, Kathleen W.

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Microarray analysis for constitutional cytogenetic abnormalities von Shaffer, Lisa G, Beaudet, Arthur L, Brothman, Arthur R, Hirsch, Betsy, Levy, Brynn, Martin, Christa Lese, Mascarello, James T, Rao, Kathleen W

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Neurological aspects of del(1q) syndrome von Murayama, Keiko, Greenwood, Robert S., Rao, Kathleen W., Aylsworth, Arthur S.

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As currently formulated, ISCN FISH nomenclature make it not practical for use in clinical test reports or cytogenetic databases von Mascarello, James T., Cooley, Linda D., Davison, Keri, Dewald, Gordon W., Brothman, Arthur R., Herrman, Marille, Park, Jonathan P., Persons, Diane L., Rao, Kathleen W., Schneider, Nancy R., Vance, Gail H.

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45X/46X,r(X) with syndactyly and severe mental retardation von Kushnick, Theodore, Irons, Thomas G., Wiley, John E., Gettig, Elizabeth A., Rao, Kathleen W., Bowyer, Susan, Opitz, John M., Reynolds, James F.

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Paracentric inversions in humans: A review of 446 paracentric inversions with presentation of 120 new cases von Pettenati, M. J., Rao, P. N., Phelan, M. C., Grass, F., Rao, K. W., Cosper, P., Carroll, A. J., Elder, F., Smith, J. L., Higgins, M. D., Lanman, J. T., Higgins, R. R., Butler, M. G., Luthardt, F., Keitges, E., Jackson-Cook, C., Brown, J., Schwartz, S., van Dyke, D. L., Palmer, C. G.

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A molecular deletion of distal chromosome 4p in two families with a satellited chromosome 4 lacking the Wolf-Hirschhorn syndrome phenotype von ESTABROOKS, L. L, LAMB, A. N, KIRKMAN, H. N, CALLANAN, N. P, RAO, K. W

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Preliminary phenotypic map of chromosome 4p16 based on 4p deletions von Estabrooks, Laurel L., Rao, Kathleen W., Driscoll, Deborah A., Crandall, Barbara F., Dean, John C. S., Ikonen, Elina, Korf, Bruce, Aylsworth, Arthur S.

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