Haploinsufficiency of HDAC4 Causes Brachydactyly Mental Retardation Syndrome, with Brachydactyly Type E, Developmental Delays, and Behavioral Problems von Williams, Stephen R., Aldred, Micheala A., Der Kaloustian, Vazken M., Halal, Fahed, Gowans, Gordon, McLeod, D. Ross, Zondag, Sara, Toriello, Helga V., Magenis, R. Ellen, Elsea, Sarah H.

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Angelman syndrome 2005: Updated consensus for diagnostic criteria von Williams, Charles A., Beaudet, Arthur L., Clayton-Smith, Jill, Knoll, Joan H., Kyllerman, Martin, Laan, Laura A., Magenis, R. Ellen, Moncla, Ann, Schinzel, Albert A., Summers, Jane A., Wagstaff, Joseph

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Hematopathologic and cytogenetic findings in imatinib mesylate–treated chronic myelogenous leukemia patients: 14 months' experience von Braziel, Rita M., Launder, Teresa M., Druker, Brian J., Olson, Susan B., Magenis, R. Ellen, Mauro, Michael J., Sawyers, Charles L., Paquette, Ronald L., O'Dwyer, Michael E.

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Amphetamine, 3,4-Methylenedioxymethamphetamine, Lysergic Acid Diethylamide, and Metabolites of the Catecholamine Neurotransmitters Are Agonists of a Rat Trace Amine Receptor von Bunzow, J R, Sonders, M S, Arttamangkul, S, Harrison, L M, Zhang, G, Quigley, D I, Darland, T, Suchland, K L, Pasumamula, S, Kennedy, J L, Olson, S B, Magenis, R E, Amara, S G, Grandy, D K

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Specific extra chromosomes occur in a modal number dependent pattern in pediatric acute lymphoblastic leukemia von Heerema, Nyla A., Raimondi, Susana C., Anderson, James R., Biegel, Jaclyn, Camitta, Bruce M., Cooley, Linda D., Gaynon, Paul S., Hirsch, Betsy, Magenis, R. Ellen, McGavran, Loris, Patil, Shivanand, Pettenati, Mark J., Pullen, Jeanette, Rao, Kathleen, Roulston, Diane, Schneider, Nancy R., Shuster, Jonathan J., Sanger, Warren, Sutcliffe, Maxine J., van Tuinen, Peter, Watson, Michael S., Carroll, Andrew J

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Y chromosome heterochromatin of differing lengths in two cell populations of the same individual von Akkari, Yassmine, Lawce, Helen, Kelson, Stephen, Smith, Cheree, Davis, Craig, Boyd, Luke, Ellen Magenis, R., Olson, Susan

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Review of disrupted sleep patterns in Smith-Magenis syndrome and normal melatonin secretion in a patient with an atypical interstitial 17p11.2 deletion von Boudreau, Eilis A., Johnson, Kyle P., Jackman, Angela R., Blancato, Jan, Huizing, Marjan, Bendavid, Claude, Jones, MaryPat, Chandrasekharappa, Settara C., Lewy, Alfred J., Smith, Ann C.M., Magenis, R. Ellen

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RAI1 point mutations, CAG repeat variation, and SNP analysis in non-deletion Smith-Magenis syndrome von Bi, Weimin, Saifi, G. Mustafa, Girirajan, Santhosh, Shi, Xin, Szomju, Barbara, Firth, Helen, Magenis, R. Ellen, Potocki, Lorraine, Elsea, Sarah H., Lupski, James R.

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SNRPN methylation patterns in germ cell tumors as a reflection of primordial germ cell development von Bussey, Kimberly J., Lawce, Helen J., Himoe, Eleanor, Shu, Xiao Ou, Heerema, Nyla A., Perlman, Elizabeth J., Olson, Susan B., Magenis, R. Ellen

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Meiotic exchange event within the stalk region of an inverted chromosome 22 results in a recombinant chromosome with duplication of the distal long arm von Boyd, Luke J., Livingston, Joseph S., Brown, Michael G., Lawce, Helen J., Gilhooly, Joseph T., Wildin, Robert S., Linck, Leesa M., Magenis, R. Ellen, Pillers, De‐Ann M.

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DNA Cross-Linker–Induced G2/M Arrest in Group C Fanconi Anemia Lymphoblasts Reflects Normal Checkpoint Function von Heinrich, Michael C., Hoatlin, Maureen E., Zigler, Amy J., Silvey, Kirsten V., Bakke, Antony C., Keeble, Winifred W., Zhi, Yu, Reifsteck, Carol A., Grompe, Markus, Brown, Michael G., Ellen Magenis, R., Olson, Susan B., Bagby, Grover C.

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Mosaicism of proximal 15q duplication/deletion resulting in Prader-Willi syndrome with normal methylation von Boyd, Luke, Brown, Michael G., Kelson, Stephen, Lawce, Helen, Shuttleworth, Sarah, Unsworth, Nancy, Magenis, R. Ellen

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Cytogenetic analysis of a primary bone angiosarcoma von Dunlap, Jennifer B, Magenis, R. Ellen, Davis, Craig, Himoe, Eleanor, Mansoor, Atiya

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Chromosomal localization of three human D5 dopamine receptor genes von Grandy, David K., Allen, Lee J., Zhang, Yuan, Magenis, R.Ellen, Civelli, Olivier

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Cytogenetic analysis of a hemosiderotic fibrolipomatous tumor von Wettach, George R, Boyd, Luke J, Lawce, Helen J, Magenis, R. Ellen, Mansoor, Atiya

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Characterization and organization of DNA sequences adjacent to the human telomere associated repeat (TTAGGG)n von WEBER, B, COLLINS, C, ROBBINS, C, MAGENIS, R. E, DELANEY, A. D, GRAY, J. W, HAYDEN, M. R

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Chromosome abnormalities of eighty-one pediatric germ cell tumors: Sex-, age-, site-, and histopathology-related differences-a Children's Cancer Group study von Bussey, Kimberly J., Lawce, Helen J., Olson, Susan B., Arthur, Diane C., Kalousek, Dagmar K., Krailo, Mark, Giller, Roger, Heifetz, Stephen, Womer, Rick, Magenis, R. Ellen

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Inherited Chondrodysplasia Punctata Due to a Deletion of the Terminal Short Arm of an X Chromosome von Curry, Cynthia J. R, Magenis, R. Ellen, Brown, Michael, Lanman, Joseph T, Tsai, Joseph, O'Lague, Patricia, Goodfellow, Peter, Mohandas, T, Bergner, E. Ann, Shapiro, Larry T

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DNA Cross-Linker–Induced G2/M Arrest in Group C Fanconi Anemia Lymphoblasts Reflects Normal Checkpoint Function von Heinrich, Michael C., Hoatlin, Maureen E., Zigler, Amy J., Silvey, Kirsten V., Bakke, Antony C., Keeble, Winifred W., Zhi, Yu, Reifsteck, Carol A., Grompe, Markus, Brown, Michael G., Ellen Magenis, R., Olson, Susan B., Bagby, Grover C.

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Molecular analysis of the Smith-Magenis syndrome : a possible contiguous-gene syndrome associated with del(17)(p11.2) von GREENBERG, F, GUZZETTA, V, MONTES DE OTA-LUNA, R, MAGENIS, R. E, SMITH, A. C. M, RICHTER, S. F, KONDO, I, DOBYNS, W. B, PATEL, P. I, LUPSKI, J. R

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