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There are 13969 results for: content related to: Association of Piebaldism, Multiple Café-au-lait Macules, and Intertriginous Freckling: Clinical Evidence of a Common Pathway between KIT and Sprouty-Related, Ena/Vasodilator-Stimulated Phosphoprotein Homology-1 Domain Containing Protein 1 (SPRED1)

  1. Café-au-lait macules and intertriginous freckling in piebaldism: Clinical overlap with neurofibromatosis type 1 and Legius syndrome

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 5, May 2012, Pages: 1195–1199, Cathy A. Stevens, Pei-Wen Chiang and Ludwine M. Messiaen

    Version of Record online : 21 MAR 2012, DOI: 10.1002/ajmg.a.35297

  2. Ultrastructural Study of Two Patients With Both Piebaldism and Neurofibromatosis 1

    Pediatric Dermatology

    Volume 10, Issue 3, September 1993, Pages: 224–234, Tsuling Chang, John D. McGrae Jr. and Ken Hashimoto

    Version of Record online : 20 MAR 2008, DOI: 10.1111/j.1525-1470.1993.tb00366.x

  3. Deletion of the SLUG (SNAI2) gene results in human piebaldism

    American Journal of Medical Genetics Part A

    Volume 122A, Issue 2, 1 October 2003, Pages: 125–132, Manuel Sánchez-Martín, Jesús Pérez-Losada, Arancha Rodríguez-García, Belén González-Sánchez, Bruce R. Korf, W. Kuster, Celia Moss, Richard A. Spritz and I. Sánchez-García

    Version of Record online : 12 JUN 2003, DOI: 10.1002/ajmg.a.20345

  4. Association of Piebaldism and Neurofibromatosis Type 1 in a Girl

    Pediatric Dermatology

    Volume 18, Issue 6, November/December 2001, Pages: 490–493, Corrado Angelo, Giuseppe Cianchini, Maria Gabriella Grosso, Giovanna Zambruno, Rino Cavalieri and Mauro Paradisi

    Version of Record online : 12 FEB 2002, DOI: 10.1046/j.1525-1470.2001.1862005.x

  5. Genetic Hypomelanoses: Disorders Characterized By Congenital White Spotting - Piebaldism, Waardenburg Syndrome, and Related Genetic Disorders of Melanocyte Development - Clinical Aspects

    The Pigmentary System: Physiology and Pathophysiology, Second Edition

    James J. Nordlund, Raymond E. Boissy, Vincent J. Hearing, Richard A. King, William S. Oetting, Jean-Paul Ortonne, Pages: 539–550, 2007

    Published Online : 26 OCT 2007, DOI: 10.1002/9780470987100.ch29

  6. Small Mammals Ignore Common Rules: A Comparison of Vocal Repertoires and the Acoustics between Pup and Adult Piebald Shrews Diplomesodon pulchellum

    Ethology

    Volume 121, Issue 2, February 2015, Pages: 103–115, Ilya A. Volodin, Alexandra S. Zaytseva, Olga G. Ilchenko and Elena V. Volodina

    Version of Record online : 25 SEP 2014, DOI: 10.1111/eth.12321

  7. Disorders of Skin Colour

    Rook's Textbook of Dermatology, Seventh Edition

    S. S. Bleehen, A. V. Anstey, Pages: 1925–1992, 2008

    Published Online : 4 FEB 2008, DOI: 10.1002/9780470750520.ch39

  8. Three novel mutations of the proto-oncogene KIT cause human piebaldism

    American Journal of Medical Genetics

    Volume 95, Issue 1, 6 November 2000, Pages: 79–81, Petros Syrris, Nasser M. Malik, Victoria A. Murday, Michael A. Patton, Nicholas D. Carter, Helen E. Hughes and Kay Metcalfe

    Version of Record online : 7 NOV 2000, DOI: 10.1002/1096-8628(20001106)95:1<79::AID-AJMG16>3.0.CO;2-4

  9. Melanoblast Development and Associated Disorders

    The Pigmentary System: Physiology and Pathophysiology, Second Edition

    James J. Nordlund, Raymond E. Boissy, Vincent J. Hearing, Richard A. King, William S. Oetting, Jean-Paul Ortonne, Pages: 140–154, 2007

    Published Online : 26 OCT 2007, DOI: 10.1002/9780470987100.ch6

  10. You have free access to this content
    In this issue

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 5, May 2012, Page: x,

    Version of Record online : 19 APR 2012, DOI: 10.1002/ajmg.a.35435

  11. You have free access to this content
    Piebaldism

    The Journal of Dermatology

    Volume 40, Issue 5, May 2013, Pages: 330–335, Naoki Oiso, Kazuyoshi Fukai, Akira Kawada and Tamio Suzuki

    Version of Record online : 1 JUN 2012, DOI: 10.1111/j.1346-8138.2012.01583.x

  12. Clonal distribution of melanocytes in piebald-spotted and variegated mice

    Journal of Experimental Zoology

    Volume 172, Issue 2, October 1969, Pages: 181–199, Robert H. Schaible

    Version of Record online : 1 JUN 2005, DOI: 10.1002/jez.1401720205

  13. De novo pericentric inversion of chromosome 4, inv(4)(p16q12) in a boy with piebaldism and mental retardation

    American Journal of Medical Genetics

    Volume 113, Issue 2, 22 November 2002, Pages: 190–192, A. Radha Ramadevi, Usha Naik, Usha Dutta, Srikanth and K. Prabhakara

    Version of Record online : 14 AUG 2002, DOI: 10.1002/ajmg.10739

  14. The Molecular Basis of Human Piebaldism

    Pigment Cell Research

    Volume 5, Issue 5, November 1992, Pages: 340–343, RICHARD A. SPRITZ

    Version of Record online : 28 JUL 2006, DOI: 10.1111/j.1600-0749.1992.tb00559.x

  15. Piebaldism: an autonomous autosomal dominant entity

    Clinical Genetics

    Volume 39, Issue 5, May 1991, Pages: 330–337, Ingrid Winship, Karen Young, Robert Martell, Rajkumar Ramesar, Diana Curtis and Peter Beighton

    Version of Record online : 28 JUN 2008, DOI: 10.1111/j.1399-0004.1991.tb03039.x

  16. Temporal skin factors influencing the development of melanoblasts in piebald mice

    Journal of Experimental Zoology

    Volume 166, Issue 3, December 1967, Pages: 397–403, Thomas C. Mayer

    Version of Record online : 1 JUN 2005, DOI: 10.1002/jez.1401660312

  17. Human piebaldism: relationship between phenotype and site of kit gene mutation

    British Journal of Dermatology

    Volume 132, Issue 6, June 1995, Pages: 929–935, K.A. WARD, C. MOSS and D.S.A. SANDERS

    Version of Record online : 6 SEP 2010, DOI: 10.1111/j.1365-2133.1995.tb16951.x

  18. The etiology and molecular genetics of human pigmentation disorders

    Wiley Interdisciplinary Reviews: Developmental Biology

    Volume 2, Issue 3, May/June 2013, Pages: 379–392, Laura L. Baxter and William J. Pavan

    Version of Record online : 17 MAY 2012, DOI: 10.1002/wdev.72

  19. Family with Legius syndrome (neurofibromatosis type 1-like syndrome)

    The Journal of Dermatology

    Volume 42, Issue 7, July 2015, Pages: 703–705, Noriyasu Sakai, Tatsuro Maeda, Hiroshi Kawakami, Masaki Uchiyama, Kazutoshi Harada, Ryoji Tsuboi and Yoshihiko Mitsuhashi

    Version of Record online : 18 MAY 2015, DOI: 10.1111/1346-8138.12862

  20. You have free access to this content
    Human piebaldism: six novel mutations of the proto-oncogene KIT

    Human Mutation

    Volume 20, Issue 3, September 2002, Page: 234, Petros Syrris, Kirsten Heathcote, Romeo Carrozzo, Koen Devriendt, Nursel Elçioglu, Christine Garrett, Meriel McEntagart and Nicholas D. Carter

    Version of Record online : 21 AUG 2002, DOI: 10.1002/humu.9057