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There are 27201 results for: content related to: Mosaic Tetrasomy 13q and Phylloid Hypomelanosis: A Case Report and Review of the Literature

  1. Tetrasomy 13q mosaicism associated with phylloid hypomelanosis and precocious puberty

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 5, May 2009, Pages: 993–996, Shweta U. Dhar, Patricia Robbins-Furman, Moise L. Levy, Ankita Patel and Fernando Scaglia

    Version of Record online : 30 MAR 2009, DOI: 10.1002/ajmg.a.32758

  2. Tetrasomy 13q31.1qter due to an inverted duplicated neocentric marker chromosome in a fetus with multiple malformations

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 4, April 2012, Pages: 894–900, Véronique Haddad, Azzedine Aboura, Lucie Tosca, Narjes Guediche, Anne-Elisabeth Mas, Aurore Coulomb L'Herminé, Luc Druart, Olivier Picone, Sophie Brisset and Gérard Tachdjian

    Version of Record online : 14 MAR 2012, DOI: 10.1002/ajmg.a.35258

  3. Phylloid Hypermelanosis: A Cutaneous Marker of Several Different Disorders?

    Pediatric Dermatology

    Volume 31, Issue 4, July/August 2014, Pages: 504–506, Rudolf Happle, Mario F. Franco-Guío and Germán Santacoloma-Osorio

    Version of Record online : 28 DEC 2012, DOI: 10.1111/pde.12053

  4. Segmental hypomelanosis and hypermelanosis arranged in a checkerboard pattern are distinct naevi: flag-like hypomelanotic naevus and flag-like hypermelanotic naevus

    Journal of the European Academy of Dermatology and Venereology

    Volume 29, Issue 11, November 2015, Pages: 2088–2099, D. Torchia and R. Happle

    Version of Record online : 6 MAR 2015, DOI: 10.1111/jdv.13077

  5. Tetrasomy 15q25[RIGHTWARDS ARROW]qter: Cytogenetic and molecular characterization of an analphoid supernumerary marker chromosome

    American Journal of Medical Genetics

    Volume 93, Issue 5, 28 August 2000, Pages: 393–398, Amy G. Rowe, Liane Abrams, Yong Qu, Emily Chen and Philip D. Cotter

    Version of Record online : 14 AUG 2000, DOI: 10.1002/1096-8628(20000828)93:5<393::AID-AJMG9>3.0.CO;2-Z

  6. Analysis of 36 Cases of Blaschkoid Dyspigmentation: Reading Between the Lines of Blaschko

    Pediatric Dermatology

    Volume 31, Issue 4, July/August 2014, Pages: 471–476, Jared Cohen III, Katayoon Shahrokh and Bernard Cohen

    Version of Record online : 14 JUL 2014, DOI: 10.1111/pde.12346

  7. Genetic Hypomelanoses: Localized Hypopigmentation

    The Pigmentary System: Physiology and Pathophysiology, Second Edition

    Wolfgang Küster, Rudolf Happle, James J. Nordlund, Jean L. Bolognia, Stella D. Calobrisi, Pranav B. Sheth, Pages: 636–656, 2007

    Published Online : 26 OCT 2007, DOI: 10.1002/9780470987100.ch32

  8. Neocentromere at 13q32 in one of two stable markers derived from a 13q21 break

    American Journal of Medical Genetics

    Volume 85, Issue 4, 6 August 1999, Pages: 385–388, H. Rivera, A.I. Vasquez, D. García-Cruz and J.A. Crolla

    Version of Record online : 8 JUL 1999, DOI: 10.1002/(SICI)1096-8628(19990806)85:4<385::AID-AJMG15>3.0.CO;2-P

  9. Genetic counselling in hypomelanosis of Ito: case report and review

    Clinical Genetics

    Volume 34, Issue 2, August 1988, Pages: 109–115, Celia Moss and John Burn

    Version of Record online : 28 JUN 2008, DOI: 10.1111/j.1399-0004.1988.tb02845.x

  10. Progressive Macular Hypomelanosis

    Pediatric Dermatology

    Volume 29, Issue 4, July/August 2012, Pages: 460–462, Maria L. Martínez-Martínez, Jose M. Azaña-Defez, Maria Rodríguez-Vázquez, Cristina Faura-Berruga and Eduardo Escario-Travesedo

    Version of Record online : 13 OCT 2011, DOI: 10.1111/j.1525-1470.2011.01506.x

  11. Hypomelanosis of Ito: No entity, but a cutaneous sign of mosaicism

    American Journal of Medical Genetics

    Volume 85, Issue 4, 6 August 1999, Pages: 346–350, Wolfgang Küster and Arne König

    Version of Record online : 8 JUL 1999, DOI: 10.1002/(SICI)1096-8628(19990806)85:4<346::AID-AJMG7>3.0.CO;2-1

  12. Cytogenetic and dermatoglyphic findings in a familial case of hypomelanosis of Ito (incontinentia pigmenti achromians)

    Clinical Genetics

    Volume 41, Issue 6, June 1992, Pages: 309–314, Walter Vormittag, Christian Ensinger and Manfred Raff

    Version of Record online : 28 JUN 2008, DOI: 10.1111/j.1399-0004.1992.tb03404.x

  13. Chromosome mosaicism in hypomelanosis of Ito

    American Journal of Medical Genetics

    Volume 35, Issue 1, January 1990, Pages: 14–17, Catherine L. Ritter, Mark W. Steele, Sharon L. Wenger and Bernard A. Cohen

    Version of Record online : 3 JUN 2005, DOI: 10.1002/ajmg.1320350104

  14. Griscelli Syndrome Type 3: Two New Cases and Review of the Literature

    Pediatric Dermatology

    Volume 32, Issue 6, November/December 2015, Pages: e245–e248, Ariella Nouriel, Jonah Zisquit, Alexander M. Helfand, Yair Anikster and Shoshana Greenberger

    Version of Record online : 4 SEP 2015, DOI: 10.1111/pde.12663

  15. 15q overgrowth syndrome: A newly recognized phenotype associated with overgrowth, learning difficulties, characteristic facial appearance, renal anomalies and increased dosage of distal chromosome 15q

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 2, February 2009, Pages: 147–154, Katrina Tatton-Brown, Daniela T. Pilz, Karen Helene Örstavik, Michael Patton, John C.K. Barber, Morag N. Collinson, Vivienne K. Maloney, Shuwen Huang, John A. Crolla, Karen Marks, Eli Ormerod, Peter Thompson, Zafar Nawaz, Christa Lese-Martin, Susan Tomkins, Paula Waits, Nazneen Rahman and Meriel McEntagart

    Version of Record online : 9 JAN 2009, DOI: 10.1002/ajmg.a.32534

  16. Hypomelanosis of Ito with Sturge–Weber Syndrome-like Leptomeningeal Angiomatosis

    Pediatric Dermatology

    Volume 19, Issue 6, November 2002, Pages: 536–540, María Pilar García Muret, Lluís Puig, Christophe Allard and Augustín Alomar

    Version of Record online : 23 NOV 2002, DOI: 10.1046/j.1525-1470.2002.00228.x

  17. 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

  18. Idiopathic guttate hypomelanosis: an electron microscopy study

    Journal of the European Academy of Dermatology and Venereology

    Volume 29, Issue 7, July 2015, Pages: 1435–1438, M. Kakepis, S. Havaki, A. Katoulis, A. Katsambas, N. Stavrianeas and T.G. Troupis

    Version of Record online : 3 AUG 2014, DOI: 10.1111/jdv.12646

  19. Structural hair shaft abnormalities in hypomelanosis of Ito and other ectodermal dysplasias

    Acta Paediatrica

    Volume 89, Issue 5, May 2000, Pages: 610–612, E Selvaag, AL Maseng Aas and S Heide

    Version of Record online : 2 JAN 2007, DOI: 10.1111/j.1651-2227.2000.tb00348.x

  20. Hypomelanosis of Ito/Pigmentary Mosaicism

    Harper's Textbook of Pediatric Dermatology, Volume 1, 2, Third Edition

    Saleem M. Taibjee, Celia Moss, Pages: 131.1–131.6, 2011

    Published Online : 24 MAY 2011, DOI: 10.1002/9781444345384.ch131