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There are 17468 results for: content related to: ‘Deletion rescue’ by mitotic 11q uniparental disomy in a family with recurrence of 11q deletion Jacobsen syndrome

  1. You have free access to this content
    Unique gene expression and clinical characteristics are associated with the 11q23 deletion in chronic lymphocytic leukaemia

    British Journal of Haematology

    Volume 128, Issue 4, February 2005, Pages: 460–471, John D. Dickinson, Lynette M. Smith, Warren G. Sanger, Guimei Zhou, Peter Townley, James C. Lynch, Z. Steven Pavletic, Philip J. Bierman and Shantaram S. Joshi

    Version of Record online : 20 JAN 2005, DOI: 10.1111/j.1365-2141.2004.05344.x

  2. Partial trisomy of 11q23.3-q25 inherited from a maternal low-level mosaic unbalanced translocation

    American Journal of Medical Genetics Part A

    Volume 167, Issue 8, August 2015, Pages: 1859–1864, Jungyoon Choi, Hojung Lee and Cha Gon Lee

    Version of Record online : 5 MAY 2015, DOI: 10.1002/ajmg.a.36980

  3. Congenital diaphragmatic hernia associated with duplication of 11q23-qter

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 14, 15 July 2006, Pages: 1580–1586, M. Klaassens, D.A. Scott, M. van Dooren, R. Hochstenbach, H.J. Eussen, W.W. Cai, R.J. Galjaard, C. Wouters, M. Poot, J. Laudy, B. Lee, D. Tibboel and A. de Klein

    Version of Record online : 12 JUN 2006, DOI: 10.1002/ajmg.a.31321

  4. Upper airway malformation associated with partial trisomy 11q

    American Journal of Medical Genetics Part A

    Volume 120A, Issue 3, 30 July 2003, Pages: 331–337, Hui-quan Zhao, Alan F. Rope, Howard M. Saal, Ruthann I. Blough-Pfau and Robert J. Hopkin

    Version of Record online : 9 APR 2003, DOI: 10.1002/ajmg.a.20134

  5. Karyotype–phenotype insights from 11q14.1-q23.2 interstitial deletions: FZD4 haploinsufficiency and exudative vitreoretinopathy in a patient with a complex chromosome rearrangement

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 24, 15 December 2006, Pages: 2721–2729, Peining Li, Hui Z. Zhang, Shannon Huff, Manjunath Nimmakayalu, Mazin Qumsiyeh, Jingwei Yu, Anna Szekely, Tian Xu and Barbara R. Pober

    Version of Record online : 13 NOV 2006, DOI: 10.1002/ajmg.a.31498

  6. Molecular characterization of an 11q interstitial deletion in a patient with the clinical features of Jacobsen syndrome

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 7, 1 April 2006, Pages: 704–708, Sharon L. Wenger, Paul D. Grossfeld, Benjamin L. Siu, James E. Coad, Frank G. Keller and Marybeth Hummel

    Version of Record online : 24 FEB 2006, DOI: 10.1002/ajmg.a.31146

  7. The 11q terminal deletion disorder: A prospective study of 110 cases

    American Journal of Medical Genetics Part A

    Volume 129A, Issue 1, 15 August 2004, Pages: 51–61, Paul D. Grossfeld, Teresa Mattina, Zona Lai, Remi Favier, Ken Lyons Jones, Finbarr Cotter and Christopher Jones

    Version of Record online : 11 JUN 2004, DOI: 10.1002/ajmg.a.30090

  8. A new case of de novo 11q duplication in a patient with normal development and intelligence and review of the literature

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 3, 1 February 2007, Pages: 265–270, Yuri A. Zarate, Jillene M. Kogan, Elizabeth K. Schorry, Teresa A. Smolarek and Robert J. Hopkin

    Version of Record online : 11 JAN 2007, DOI: 10.1002/ajmg.a.31519

  9. Deletion of 11q23 is a frequent event in the evolution of MYCN single-copy high-risk neuroblastomas

    Medical and Pediatric Oncology

    Volume 35, Issue 6, 1 December 2000, Pages: 544–546, Chun Guo, Peter S. White, Michael D. Hogarty, Garrett M. Brodeur, Robert Gerbing, Daniel O. Stram and John M. Maris

    Version of Record online : 30 NOV 2000, DOI: 10.1002/1096-911X(20001201)35:6<544::AID-MPO10>3.0.CO;2-2

  10. Identification and molecular characterization of a small 11q23.3 de novo duplication in a patient with Rett syndrome manifestations

    American Journal of Medical Genetics

    Volume 80, Issue 3, 16 November 1998, Pages: 273–280, Bruno Delobel, Valérie Delannoy, Giorgio Pini, Michele Zapella, Marc Tardieu, Louis Vallée and Marie F. Croquette

    Version of Record online : 15 DEC 1998, DOI: 10.1002/(SICI)1096-8628(19981116)80:3<273::AID-AJMG19>3.0.CO;2-6

  11. Genetic Features of B-Cell Chronic Lymphocytic Leukemia

    Reviews in Clinical and Experimental Hematology

    Volume 4, Issue 1, March 2000, Pages: 48–72, Stephan Stilgenbauer, Peter Lichter and Hartmut Döhner

    Version of Record online : 9 OCT 2008, DOI: 10.1046/j.1468-0734.2000.00003.x

  12. Characterization of chromosome 11 breakpoints and the areas of deletion and amplification in patients with newly diagnosed acute myeloid leukemia

    Genes, Chromosomes and Cancer

    Volume 52, Issue 7, July 2013, Pages: 619–635, Iveta Sarova, Jana Brezinova, Zuzana Zemanova, Dagmar Bystricka, Zdenek Krejcik, Petr Soukup, Jan Vydra, Jaroslav Cermak, Anna Jonasova and Kyra Michalova

    Version of Record online : 12 APR 2013, DOI: 10.1002/gcc.22058

  13. You have free access to this content
    Chromosomes, 11q and cancer: a review

    The Journal of Pathology

    Volume 187, Issue 1, January 1999, Pages: 28–38, John Koreth, Christopher J. Bakkenist and James O'D. McGee

    Version of Record online : 24 SEP 1999, DOI: 10.1002/(SICI)1096-9896(199901)187:1<28::AID-PATH166>3.0.CO;2-R

  14. Familial interstitial duplication of 11q; partial trisomy (11)(q13.5q21)

    American Journal of Medical Genetics Part A

    Volume 126A, Issue 4, 1 May 2004, Pages: 423–426, Krishna K. Yelavarthi and Janice Zunich

    Version of Record online : 26 NOV 2003, DOI: 10.1002/ajmg.a.20610

  15. You have free access to this content
    Identification of two distinct deletion targets at 11q23 in cutaneous malignant melanoma

    International Journal of Cancer

    Volume 80, Issue 2, 18 January 1999, Pages: 205–209, Rudolf A. Herbst, Ralf Gutzmer, Frank Matiaske, Susanne Mommert, Uta Casper, Alexer Kapp and Jürgen Weiss

    Version of Record online : 8 NOV 1999, DOI: 10.1002/(SICI)1097-0215(19990118)80:2<205::AID-IJC8>3.0.CO;2-J

  16. Giant platelets in a case of deletion 11q24-qter confirmed by fluorescence in situ hybridization

    American Journal of Medical Genetics

    Volume 110, Issue 2, 15 June 2002, Pages: 170–175, Anatole Laleye, Daniele Delneste, Olivier Pradier, Christine Hans, Raphaël Darboux and Gonul Ogur

    Version of Record online : 25 APR 2002, DOI: 10.1002/ajmg.10418

  17. FISH analyses for alterations in chromosomes 1, 2, 3, and 11 define high-risk groups in neuroblastoma

    Medical and Pediatric Oncology

    Volume 41, Issue 1, July 2003, Pages: 30–35, Ruediger Spitz, Barbara Hero, Karen Ernestus and Frank Berthold

    Version of Record online : 16 MAY 2003, DOI: 10.1002/mpo.10313

  18. Distinct sequences on 11q13.5 and 11q23–24 are frequently coamplified with MLL in complexly organized 11q amplicons in AML/MDS patients

    Genes, Chromosomes and Cancer

    Volume 39, Issue 4, April 2004, Pages: 263–276, Andrea Zatkova, Reinhard Ullmann, Jean Marie Rouillard, Barbara J. Lamb, Rork Kuick, Sam M. Hanash, Susanne Schnittger, Claudia Schoch, Christa Fonatsch and Katharina Wimmer

    Version of Record online : 22 JAN 2004, DOI: 10.1002/gcc.20002

  19. You have free access to this content
    Impact of trisomy 12, del(13q), del(17p), and del(11q) on the immunophenotype, DNA ploidy status, and proliferative rate of leukemic B-cells in chronic lymphocytic leukemia

    Cytometry Part B: Clinical Cytometry

    Volume 74B, Issue 3, May 2008, Pages: 139–149, Sandra Quijano, Antonio López, Ana Rasillo, José María Sayagués, Susana Barrena, Maria Luz Sánchez, Cristina Teodosio, Pilar Giraldo, Manuel Giralt, M. Carmen Pérez, Mercedes Romero, Luis Perdiguer and Alberto Orfao

    Version of Record online : 5 DEC 2007, DOI: 10.1002/cyto.b.20390

  20. Molecular cytogenetics localizes two new breakpoints on 11q23.3 and 21q11.2 in myelodysplastic syndrome with t(11;21) translocation

    Genes, Chromosomes and Cancer

    Volume 24, Issue 3, March 1999, Pages: 199–206, Iwona Wlodarska, Licia Selleri, Roberta La Starza, Caroline Paternotte, Glen A. Evans, Marc Boogaerts, Herman Van den Berghe and Cristina Mecucci

    Version of Record online : 8 FEB 1999, DOI: 10.1002/(SICI)1098-2264(199903)24:3<199::AID-GCC4>3.0.CO;2-V