Search Results

There are 1434918 results for: content related to: Chromosome 19p13.3 deletion in a patient with macrocephaly, obesity, mental retardation, and behavior problems

  1. Distinct phenotype associated with a cryptic subtelomeric deletion of 19p13.3-pter

    American Journal of Medical Genetics Part A

    Volume 136A, Issue 1, 1 July 2005, Pages: 38–44, H.L. Archer, S. Gupta, S. Enoch, P. Thompson, A. Rowbottom, I. Chua, S. Warren, D. Johnson, D.H. Ledbetter, C. Lese-Martin, P. Williams and D.T. Pilz

    Article first published online : 3 JUN 2005, DOI: 10.1002/ajmg.a.30774

  2. Abnormal lysosomal and ubiquitin-proteasome pathways in 19p13.3 distal myopathy

    Annals of Neurology

    Volume 56, Issue 1, July 2004, Pages: 133–138, Claudia Di Blasi, Behzad Moghadaszadeh, Claudia Ciano, Tiziana Negri, Alessio Giavazzi, Ferdinando Cornelio, Lucia Morandi and Marina Mora

    Article first published online : 28 JUN 2004, DOI: 10.1002/ana.20158

  3. Molecular characterization of a novel, de novo, cryptic interstitial deletion on 19p13.3 in a child with a cutis aplasia and multiple congenital anomalies

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 12, December 2010, Pages: 3148–3153, Hussam Al-Kateb, Amanda Hahn, Julie M. Gastier-Foster, Linda Jeng, Shawn E. McCandless and Christine A. Curtis

    Article first published online : 24 NOV 2010, DOI: 10.1002/ajmg.a.33738

  4. Molecular cytogenetic characterization of TCF3 (E2A)/19p13.3 rearrangements in B-cell precursor acute lymphoblastic leukemia

    Genes, Chromosomes and Cancer

    Volume 46, Issue 5, May 2007, Pages: 478–486, Kerry E. Barber, Christine J. Harrison, Zoe J. Broadfield, Adam R. M. Stewart, Sarah L. Wright, Mary Martineau, Jon C. Strefford and Anthony V. Moorman

    Article first published online : 20 FEB 2007, DOI: 10.1002/gcc.20431

  5. Spinocerebellar ataxia type 26 maps to chromosome 19p13.3 adjacent to SCA6

    Annals of Neurology

    Volume 57, Issue 3, March 2005, Pages: 349–354, Guo-Yun Yu, Michael J. Howell, Matthew J. Roller, Ting-Dong Xie and Christopher M. Gomez

    Article first published online : 24 FEB 2005, DOI: 10.1002/ana.20371

  6. You have full text access to this OnlineOpen article
    Recurrent deletions of the TNFSF7 and TNFSF9 genes in 19p13.3 in diffuse large B-cell and Burkitt lymphomas

    International Journal of Cancer

    Volume 131, Issue 5, 1 September 2012, Pages: E830–E835, René Scholtysik, Inga Nagel, Markus Kreuz, Inga Vater, Maciej Giefing, Carsten Schwaenen, Swen Wessendorf, Lorenz Trümper, Markus Loeffler, Reiner Siebert and Ralf Küppers

    Article first published online : 31 JAN 2012, DOI: 10.1002/ijc.27416

  7. Partial trisomy 19p13.3 and partial monosomy 1p36.3: Clinical report and a literature review

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 8, August 2009, Pages: 1782–1785, Surasak Puvabanditsin, Eugene Garrow, Erik Brandsma, Jayshree Savla, Bgee Kunjumon and Inder Gadi

    Article first published online : 16 JUL 2009, DOI: 10.1002/ajmg.a.32972

  8. 11q23 balanced chromosome aberrations in treatment-related myelodysplastic syndromes and acute leukemia: Report from an International Workshop

    Genes, Chromosomes and Cancer

    Volume 33, Issue 4, April 2002, Pages: 362–378, Clara D. Bloomfield, Kellie J. Archer, Krzysztof Mrózek, Debra M. Lillington, Yasuhiko Kaneko, David R. Head, Paola Dal Cin and Susana C. Raimondi

    Article first published online : 31 DEC 2001, DOI: 10.1002/gcc.10046

  9. Gastric cancers in young and elderly patients show different genomic profiles

    The Journal of Pathology

    Volume 211, Issue 1, January 2007, Pages: 45–51, TE Buffart, B Carvalho, E Hopmans, V Brehm, E Klein Kranenbarg, TBM Schaaij-Visser, PP Eijk, NCT van Grieken, B Ylstra, CJH van de Velde and GA Meijer

    Article first published online : 20 NOV 2006, DOI: 10.1002/path.2085

  10. Genomic aberrations in pediatric gliomas and embryonal tumors

    Genes, Chromosomes and Cancer

    Volume 50, Issue 10, October 2011, Pages: 788–799, Hanne-Sofie S. Dahlback, Petter Brandal, Ludmila Gorunova, Eva Widing, Torstein R. Meling, Bård K. Krossnes and Sverre Heim

    Article first published online : 29 JUN 2011, DOI: 10.1002/gcc.20898

  11. Analysis of myelodysplastic syndromes with complex karyotypes by high-resolution comparative genomic hybridization and subtelomeric CGH array

    Genes, Chromosomes and Cancer

    Volume 42, Issue 3, March 2005, Pages: 287–298, Angel Martínez-Ramírez, Miguel Urioste, Lorenzo Melchor, David Blesa, Laura Valle, Sara Alvarez de Andrés, Klaas Kok, Maria José Calasanz, Juan Cruz Cigudosa and Javier Benítez

    Article first published online : 20 DEC 2004, DOI: 10.1002/gcc.20154

  12. Suggestive linkage to chromosome 19 in a large Cuban family with late-onset Parkinson's disease

    Movement Disorders

    Volume 18, Issue 11, November 2003, Pages: 1240–1249, Aida M. Bertoli-Avella, Jose L. Giroud-Benitez, Vincenzo Bonifati, Eduardo Alvarez-Gonzalez, Luis Heredero-Baute, Cornelia M. Van Duijn and Peter Heutink

    Article first published online : 8 JUL 2003, DOI: 10.1002/mds.10534

  13. Genome-wide linkage scan for breast cancer susceptibility loci in Swedish hereditary non-BRCA1/2 families: Suggestive linkage to 10q23.32-q25.3

    Genes, Chromosomes and Cancer

    Volume 46, Issue 3, March 2007, Pages: 302–309, Annika Bergman, Per Karlsson, Jonna Berggren, Tommy Martinsson, Karin Björck, Staffan Nilsson, Jan Wahlström, Arne Wallgren and Margareta Nordling

    Article first published online : 14 DEC 2006, DOI: 10.1002/gcc.20405

  14. Adrenocortical carcinoma is characterized by a high frequency of chromosomal gains and high-level amplifications

    Genes, Chromosomes and Cancer

    Volume 28, Issue 2, June 2000, Pages: 145–152, Martha Dohna, Martin Reincke, Antoaneta Mincheva, Bruno Allolio, Sabina Solinas-Toldo and Peter Lichter

    Article first published online : 22 MAY 2000, DOI: 10.1002/(SICI)1098-2264(200006)28:2<145::AID-GCC3>3.0.CO;2-7

  15. Allelic loss and gain, but not genomic instability, as the major somatic mutation in primary hepatocellular carcinoma

    Genes, Chromosomes and Cancer

    Volume 31, Issue 3, July 2001, Pages: 221–227, Gang Wang, Yan Zhao, Xiaoming Liu, Lu Wang, Chungen Wu, Weiling Zhang, Wanqing Liu, Pingping Zhang, Wenming Cong, Yuanrong Zhu, Lisheng Zhang, Saijuan Chen, Dafang Wan, Xintai Zhao, Wei Huang and Jianren Gu

    Article first published online : 27 APR 2001, DOI: 10.1002/gcc.1138

  16. Microarray-based gene expression analysis of human osteoblasts in response to different biomaterials

    Journal of Biomedical Materials Research Part A

    Volume 88A, Issue 2, February 2009, Pages: 401–408, Karina F. Bombonato-Prado, Larissa S. Bellesini, Cristina M. Junta, Márcia M. Marques, Geraldo A. Passos and Adalberto L. Rosa

    Article first published online : 27 FEB 2008, DOI: 10.1002/jbm.a.31701

  17. You have free access to this content
    A novel chromosome 19p13.12 deletion in a child with multiple congenital anomalies

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 3, March 2009, Pages: 396–402, Daniel R. Jensen, Donna M. Martin, Stephen Gebarski, Trilochan Sahoo, Ellen K. Brundage, A. Craig Chinault, Edgar A. Otto, Moumita Chaki, Friedhelm Hildebrandt, Sau Wai Cheung and Marci M. Lesperance

    Article first published online : 12 FEB 2009, DOI: 10.1002/ajmg.a.32691

  18. Three-way translocation involves MLL, MLLT3, and a novel cell cycle control gene, FLJ10374, in the pathogenesis of acute myeloid leukemia with t(9;11;19)(p22;q23;p13.3)

    Genes, Chromosomes and Cancer

    Volume 45, Issue 5, May 2006, Pages: 455–469, Luís Vieira, Ana C. Sousa, Paulo Matos, Bárbara Marques, Helena Alaiz, Maria J. Ribeiro, Paula Braga, Maria G. da Silva and Peter Jordan

    Article first published online : 31 JAN 2006, DOI: 10.1002/gcc.20311

  19. You have full text access to this OnlineOpen article
    Homozygosity for the 168His variant of the minor histocompatibility antigen HA-1 is associated with reduced risk of primary Sjögren's syndrome

    European Journal of Immunology

    Volume 35, Issue 1, January 2005, Pages: 305–317, Mariann Harangi, Wolfgang E. Kaminski, Martin Fleck, Evelyn Orsó, Margit Zeher, Emese Kiss, Zoltán Szekanecz, Erika Zilahi, Jörg Marienhagen, Charalampos Aslanidis, György Paragh, Anne Isine Bolstad, Roland Jonsson and Gerd Schmitz

    Article first published online : 10 DEC 2004, DOI: 10.1002/eji.200425406

  20. Concurrent translocations of MLL and CBFA2 (AML1) genes with new partner breakpoints in a child with secondary myelodysplastic syndrome after treatment of acute lymphoblastic leukemia

    Genes, Chromosomes and Cancer

    Volume 28, Issue 2, June 2000, Pages: 227–232, Susan Mathew, David Head, Jeffrey E. Rubnitz and Susana C. Raimondi

    Article first published online : 22 MAY 2000, DOI: 10.1002/(SICI)1098-2264(200006)28:2<227::AID-GCC12>3.0.CO;2-J