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There are 16726 results for: content related to: Partial trisomy 19p13.3 and partial monosomy 1p36.3: Clinical report and a literature review

  1. Submicroscopic deletion 9(q34.4) and duplication 19(p13.3): Identified by subtelomere specific FISH probes

    American Journal of Medical Genetics Part A

    Volume 125A, Issue 1, 15 February 2004, Pages: 67–72, Denise I. Quigley, Kathleen Kaiser-Rogers, Arthur S. Aylsworth and Kathleen W. Rao

    Version of Record online : 29 AUG 2003, DOI: 10.1002/ajmg.a.20457

  2. Cryptic 1p36.3/6q25.2 translocation in three generations ascertained through a foetus with IUGR and cerebral malformations

    Prenatal Diagnosis

    Volume 23, Issue 10, October 2003, Pages: 819–823, S. Cavani, C. Perfumo, F. Faravelli, M. Malacarne, M. Sogliani, G. Piombo, G. Zerega, M. Zucca, F. Dagna Bricarelli and M. Pierluigi

    Version of Record online : 4 SEP 2003, DOI: 10.1002/pd.678

  3. Partial trisomy 19p: case report and natural history

    Clinical Genetics

    Volume 41, Issue 3, March 1992, Pages: 143–146, B. A. Salbert, M. Solomon, J. L. Spence, C. Jackson-Cook, J. Brown and J. Bodurtha

    Version of Record online : 28 JUN 2008, DOI: 10.1111/j.1399-0004.1992.tb03651.x

  4. Clinical presentation of 13 patients with subtelomeric rearrangements and a review of the literature

    American Journal of Medical Genetics Part A

    Volume 128A, Issue 4, 1 August 2004, Pages: 352–363, Amy E. Roberts, Gerald F. Cox, Virginia Kimonis, Allen Lamb and Mira Irons

    Version of Record online : 6 JUL 2004, DOI: 10.1002/ajmg.a.30142

  5. You have free access to this content
    The Human Obesity Gene Map: The 2005 Update

    Obesity

    Volume 14, Issue 4, April 2006, Pages: 529–644, Tuomo Rankinen, Aamir Zuberi, Yvon C. Chagnon, S. John Weisnagel, George Argyropoulos, Brandon Walts, Louis Pérusse and Claude Bouchard

    Version of Record online : 6 SEP 2012, DOI: 10.1038/oby.2006.71

  6. Partial monosomy of chromosome 1p36.3: Characterization of the critical region and delineation of a syndrome

    American Journal of Medical Genetics

    Volume 59, Issue 4, 4 December 1995, Pages: 467–475, Orit Reish, Susan A. Berry and Betsy Hirsch

    Version of Record online : 16 MAY 2005, DOI: 10.1002/ajmg.1320590413

  7. You have free access to this content
    The Human Obesity Gene Map: The 2003 Update

    Obesity Research

    Volume 12, Issue 3, March 2004, Pages: 369–439, Eric E. Snyder, Brandon Walts, Louis Pérusse, Yvon C. Chagnon, S. John Weisnagel, Tuomo Rankinen and Claude Bouchard

    Version of Record online : 6 SEP 2012, DOI: 10.1038/oby.2004.47

  8. 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

    Version of Record online : 3 JUN 2005, DOI: 10.1002/ajmg.a.30774

  9. Reverse painting of microdissected chromosome 19 markers in ovarian carcinoma identifies a complex rearrangement map

    Genes, Chromosomes and Cancer

    Volume 48, Issue 2, February 2009, Pages: 184–193, Francesca Micci, Jörg Weimer, Lisbeth Haugom, Rolf I. Skotheim, Regina Grunewald, Vera M. Abeler, Ilvar Silins, Ragnhild A. Lothe, Claes G. Trope, Norbert Arnold and Sverre Heim

    Version of Record online : 30 OCT 2008, DOI: 10.1002/gcc.20628

  10. Primary effusion lymphoma: genomic profiling revealed amplification of SELPLG and CORO1C encoding for proteins important for cell migration

    The Journal of Pathology

    Volume 222, Issue 2, October 2010, Pages: 166–179, Shi-Lu Luan, Emmanuelle Boulanger, Hongtao Ye, Estelle Chanudet, Nicola Johnson, Rifat A Hamoudi, Chris M Bacon, Hongxiang Liu, Yuanxue Huang, Jonathan Said, Peiguo Chu, Christoph S Clemen, Ethel Cesarman, Amy Chadburn, Peter G Isaacson and Ming-Qing Du

    Version of Record online : 12 JUL 2010, DOI: 10.1002/path.2752

  11. Human-Mouse Comparative Maps

    Appendix

    Current Protocols in Human Genetics

    6:A.6.1–A.6.42

    Michael F. Seldin

    Published Online : 1 MAY 2001, DOI: 10.1002/0471142905.hga06s09

  12. Monosomy 1p36 deletion syndrome

    American Journal of Medical Genetics Part C: Seminars in Medical Genetics

    Volume 145C, Issue 4, 15 November 2007, Pages: 346–356, Marzena Gajecka, Katherine L. Mackay and Lisa G. Shaffer

    Version of Record online : 5 OCT 2007, DOI: 10.1002/ajmg.c.30154

  13. Chromogenic in situ Hybridization is a Reliable Alternative to Fluorescence in situ Hybridization for Diagnostic Testing of 1p and 19q Loss in Paraffin-Embedded Gliomas

    Brain Pathology

    Volume 23, Issue 3, May 2013, Pages: 311–318, Ulrike Lass, Christian Hartmann, David Capper, Christel Herold-Mende, Andreas von Deimling, Maren Meiboom and Wolf Mueller

    Version of Record online : 29 NOV 2012, DOI: 10.1111/bpa.12003

  14. Combined partial trisomy 11q and partial monosomy 10p in a 19-year-old female patient: Phenotypic and genotypic findings

    American Journal of Medical Genetics Part A

    Volume 155, Issue 12, December 2011, Pages: 3075–3081, Anja Hagen, Arndt Bigl, Dorothea Wand, Eva Klopocki, Raoul Heller, Manuela Siekmeyer, Werner Siekmeyer, Wieland Kiess and Andreas Merkenschlager

    Version of Record online : 3 NOV 2011, DOI: 10.1002/ajmg.a.34300

  15. Girl with monosomy 1p36 and Angelman syndrome due to unbalanced der(1) transmission of a maternal translocation t(1;15)(p36.3;q13.1)

    American Journal of Medical Genetics Part A

    Volume 131A, Issue 1, 15 November 2004, Pages: 94–98, Hiroyuki Torisu, Toshiyuki Yamamoto, Takehisa Fujiwaki, Mitsutaka Kadota, Mitsuo Oshimura, Kenji Kurosawa, Shinjiro Akaboshi and Akira Oka

    Version of Record online : 21 SEP 2004, DOI: 10.1002/ajmg.a.30413

  16. Analysis of colorectal tumor progression by microdissection and comparative genomic hybridization

    Genes, Chromosomes and Cancer

    Volume 37, Issue 4, August 2003, Pages: 369–380, Helen E. Alcock, Timothy J. Stephenson, Janice A. Royds and David W. Hammond

    Version of Record online : 7 MAY 2003, DOI: 10.1002/gcc.10201

  17. Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1–p23.1, 4q21.21–q22.1, 6q26–q27, and 21q2

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 13, 1 July 2008, Pages: 1637–1654, William B. Dobyns, Ghayda Mirzaa, Susan L. Christian, Kristin Petras, Jessica Roseberry, Gary D. Clark, Cynthia J.R. Curry, Donna McDonald-McGinn, Livija Medne, Elaine Zackai, Julie Parsons, Dina J. Zand, Fuki M. Hisama, Christopher A. Walsh, Richard J. Leventer, Christa L. Martin, Marzena Gajecka and Lisa G. Shaffer

    Version of Record online : 5 JUN 2008, DOI: 10.1002/ajmg.a.32293

  18. You have free access to this content
    The Human Obesity Gene Map: The 2004 Update

    Obesity Research

    Volume 13, Issue 3, March 2005, Pages: 381–490, Louis Pérusse, Tuomo Rankinen, Aamir Zuberi, Yvon C. Chagnon, S. John Weisnagel, George Argyropoulos, Brandon Walts, Eric E. Snyder and Claude Bouchard

    Version of Record online : 6 SEP 2012, DOI: 10.1038/oby.2005.50

  19. Segregation of a t(1;3) translocation in multiple affected family members with both types of adjacent-1 segregants

    American Journal of Medical Genetics Part A

    Volume 124A, Issue 2, 15 January 2004, Pages: 118–128, Chahira Kozma, Anne M. Slavotinek and Jeanne M. Meck

    Version of Record online : 16 JUN 2003, DOI: 10.1002/ajmg.a.20332

  20. 19p + marker chromosome correlates with relapse in malignant fibrous histiocytoma

    Genes, Chromosomes and Cancer

    Volume 16, Issue 2, June 1996, Pages: 88–93, Peter F. M. Choong, Nils Mandahl, Fredrik Mertens, Helena Willén, Thor Alvegård, Andris Kreicbergs, Felix Mitelman and Anders Rydholm

    Version of Record online : 7 DEC 1998, DOI: 10.1002/(SICI)1098-2264(199606)16:2<88::AID-GCC2>3.0.CO;2-Z