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There are 3601 results for: content related to: Differential diagnosis of Smith–Magenis syndrome: 1p36 deletion syndrome

  1. Chromosome 1

    Standard Article

    eLS

    Peter S White

    Published Online : 28 SEP 2007, DOI: 10.1002/9780470015902.a0005810.pub2

  2. 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

  3. 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

  4. 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

  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. Molecular cytogenetic characterization of a familial der(1)del(1)(p36.33)dup(1)(p36.33p36.22) with variable phenotype

    American Journal of Medical Genetics Part A

    Volume 139A, Issue 2, 1 December 2005, Pages: 136–140, Vijay S. Tonk, Golder N. Wilson, Svetlana A. Yatsenko, Pawel Stankiewicz, James R. Lupski, Robert C. Schutt, J.K. Northup and Gopalrao V.N. Velagaleti

    Version of Record online : 8 NOV 2005, DOI: 10.1002/ajmg.a.30958

  7. A high-resolution radiation hybrid map of porcine chromosome 6

    Animal Genetics

    Volume 35, Issue 5, October 2004, Pages: 367–378, H. Cao, J. A. B. Robinson, Z. Jiang, J. S. Melville, S. P. Golovan, M. W. Jones and A. M. Verrinder Gibbins

    Version of Record online : 4 AUG 2004, DOI: 10.1111/j.1365-2052.2004.01161.x

  8. Analysis of chromosomal imbalances in de novo CD5-positive diffuse large-B-cell lymphoma detected by comparative genomic hybridization

    Genes, Chromosomes and Cancer

    Volume 39, Issue 1, January 2004, Pages: 77–81, Sivasundaram Karnan, Hiroyuki Tagawa, Ritsuro Suzuki, Miyuki Suguro, Motoko Yamaguchi, Masataka Okamoto, Yasuo Morishima, Shigeo Nakamura and Masao Seto

    Version of Record online : 10 OCT 2003, DOI: 10.1002/gcc.10298

  9. Array comparative genomic hybridization analysis of chromosomal imbalances and their target genes in gastrointestinal stromal tumors

    Genes, Chromosomes and Cancer

    Volume 46, Issue 6, June 2007, Pages: 564–576, Reetta Ässämäki, Maarit Sarlomo-Rikala, José Antonio Lopez-Guerrero, Jerzy Lasota, Leif C. Andersson, Antonio Llombart-Bosch, Markku Miettinen and Sakari Knuutila

    Version of Record online : 28 FEB 2007, DOI: 10.1002/gcc.20439

  10. Smallest region of overlapping deletion in 1p36 in human neuroblastoma: A 1 Mbp cosmid and PAC contig

    Genes, Chromosomes and Cancer

    Volume 31, Issue 3, July 2001, Pages: 228–239, Anja Bauer, Larissa Savelyeva, Andreas Claas, Christian Praml, Frank Berthold and Manfred Schwab

    Version of Record online : 27 APR 2001, DOI: 10.1002/gcc.1139

  11. 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

  12. Are Angelman and Prader-Willi syndromes more similar than we thought? Food-related behavior problems in Angelman, Cornelia de Lange, Fragile X, Prader-Willi and 1p36 deletion syndromes

    American Journal of Medical Genetics Part A

    Volume 167, Issue 3, March 2015, Pages: 572–578, Alice Welham, Johnny King L. Lau, Joanna Moss, Jenny Cullen, Suzanne Higgs, Gemma Warren, Lucy Wilde, Abby Marr, Faye Cook and Chris Oliver

    Version of Record online : 18 FEB 2015, DOI: 10.1002/ajmg.a.36923

  13. Genetic and epigenetic characterization of low-grade gliomas reveals frequent methylation of the MLH3 gene

    Genes, Chromosomes and Cancer

    Volume 54, Issue 11, November 2015, Pages: 655–667, Halka Lhotska, Zuzana Zemanova, Hana Cechova, Sarka Ransdorfova, Libuse Lizcova, Filip Kramar, Zdenek Krejcik, Karla Svobodova, Dagmar Bystricka, Petr Hrabal, Alena Dohnalova and Kyra Michalova

    Version of Record online : 25 AUG 2015, DOI: 10.1002/gcc.22266

  14. Identification of a minimal region of loss on the short arm of chromosome 1 in Wilms tumor

    Genes, Chromosomes and Cancer

    Volume 46, Issue 4, April 2007, Pages: 327–335, Yahya Tamimi, Kay Ziebart, Nancy Desaulniers, Kevin Dietrich and Paul Grundy

    Version of Record online : 22 JAN 2007, DOI: 10.1002/gcc.20413

  15. 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

  16. Molecular cytogenetic analysis of cutaneous T-cell lymphomas: identification of common genetic alterations in Sézary syndrome and mycosis fungoides

    British Journal of Dermatology

    Volume 147, Issue 3, September 2002, Pages: 464–475, X. Mao, D Lillington, J.J. Scarisbrick, T. Mitchell, B. Czepulkowski, R. Russell-Jones, B. Young and S.J. Whittaker

    Version of Record online : 5 SEP 2002, DOI: 10.1046/j.1365-2133.2002.04966.x

  17. Two cases of mosaic RhD blood-group phenotypes and paternal isodisomy for chromosome 1

    American Journal of Medical Genetics

    Volume 104, Issue 3, 1 December 2001, Pages: 250–256, Osamu Miyoshi, Ryuichi Yabe, Keiko Wakui, Yoshimitsu Fukushima, Shigeki Koizumi, Makoto Uchikawa, Tadashi Kajii, Chikahiko Numakura, Shunji Takahashi, Kiyoshi Hayasaka and Norio Niikawa

    Version of Record online : 25 OCT 2001, DOI: 10.1002/ajmg.10000

  18. You have free access to this content
    Combining array-based approaches for the identification of candidate tumor suppressor loci in mature lymphoid neoplasms

    APMIS

    Volume 115, Issue 10, October 2007, Pages: 1107–1134, INGA NIELÄNDER, STEFANIE BUG, JULIA RICHTER, MACIEJ GIEFING, JOSÉ IGNACIO MARTÍN-SUBERO and REINER SIEBERT

    Version of Record online : 26 NOV 2007, DOI: 10.1111/j.1600-0463.2007.apm_883.xml.x

  19. You have free access to this content
    Identification of novel regions of amplification and deletion within mantle cell lymphoma DNA by comparative genomic hybridization

    British Journal of Haematology

    Volume 116, Issue 2, February 2002, Pages: 291–298, Jeannette E. Allen, Rachael E. Hough, John R. Goepel, Sarah Bottomley, Gill A. Wilson, Helen E. Alcock, Margaret Baird, Paul C. Lorigan, Elisabeth A. Vandenberghe, Barry W. Hancock and David W. Hammond

    Version of Record online : 1 FEB 2002, DOI: 10.1046/j.1365-2141.2002.03260.x

  20. Clinical implications of chromosomal abnormalities in gastric adenocarcinomas

    Genes, Chromosomes and Cancer

    Volume 35, Issue 3, November 2002, Pages: 219–231, Chew-Wun Wu, Gen-Der Chen, Cathy S.-J. Fann, Anna F.-Y. Lee, Chin-Wen Chi, Jacqueline M. Liu, Ulli Weier and Jeou-Yuan Chen

    Version of Record online : 26 JUN 2002, DOI: 10.1002/gcc.10106