SEARCH

SEARCH BY CITATION

Cited in:

CrossRef

This article has been cited by:

  1. 1
    Elizabeth R Heller, Sikandar G Khan, Christiane Kuschal, Deborah Tamura, John J DiGiovanna, Kenneth H Kraemer, Mutations in the TTDN1 Gene Are Associated with a Distinct Trichothiodystrophy Phenotype, Journal of Investigative Dermatology, 2015, 135, 3, 734

    CrossRef

  2. 2
    Karin E. M. Diderich, Claudia Nicolaije, Matthias Priemel, Jan H. Waarsing, Judd S. Day, Renata M. C. Brandt, Arndt F. Schilling, Sander M. Botter, Harrie Weinans, Gijsbertus T. J. van der Horst, Jan H. J. Hoeijmakers, Johannes P. T. M. van Leeuwen, Bone fragility and decline in stem cells in prematurely aging DNA repair deficient trichothiodystrophy mice, AGE, 2012, 34, 4, 845

    CrossRef

  3. You have free access to this content3
    Fanny Morice-Picard, Muriel Cario-André, Hamid Rezvani, Didier Lacombe, Alain Sarasin, Alain Taïeb, New clinico-genetic classification of trichothiodystrophy, American Journal of Medical Genetics Part A, 2009, 149A, 9
  4. 4
    Amy S. Cheng, Susan J. Bayliss, The genetics of hair shaft disorders, Journal of the American Academy of Dermatology, 2008, 59, 1, 1

    CrossRef

  5. 5
    David A. Whiting, Lady C. Dy, Office Diagnosis of Hair Shaft Defects, Seminars in Cutaneous Medicine and Surgery, 2006, 25, 1, 24

    CrossRef

  6. 6
    Kazuhiko Nakabayashi, Daniela Amann, Yan Ren, Ulpu Saarialho-Kere, Nili Avidan, Simone Gentles, Jeffrey R. MacDonald, Erik G. Puffenberger, Angela M. Christiano, Amalia Martinez-Mir, Julio C. Salas-Alanis, Renata Rizzo, Esther Vamos, Anja Raams, Clifford Les, Eric Seboun, Nicolaas G.J. Jaspers, Jacques S. Beckmann, Charles E. Jackson, Stephen W. Scherer, Identification of C7orf11 (TTDN1) Gene Mutations and Genetic Heterogeneity in Nonphotosensitive Trichothiodystrophy, The American Journal of Human Genetics, 2005, 76, 3, 510

    CrossRef

  7. 7
    Peter H. Itin, Alain Sarasin, Mark R. Pittelkow, Trichothiodystrophy: Update on the sulfur-deficient brittle hair syndromes, Journal of the American Academy of Dermatology, 2001, 44, 6, 891

    CrossRef

  8. 8
    A Richetta, S Giustini, A Rossi, S Calvieri, What’s new in trichothiodystrophy, Journal of the European Academy of Dermatology and Venereology, 2001, 15, 1
  9. 9
    Catherine L. Wetzburger, Nicole Van Regemorter, Henri B. Szliwowski, Marc J. Abramowicz, Patrick Van Bogaert, Gray matter heterotopia and acute necrotizing encephalopathy in trichothiodystrophy, Pediatric Neurology, 1998, 19, 5, 392

    CrossRef

  10. 10
    R.P.R. Dawber, AN UPDATE OF HAIR SHAFT DISORDERS, Dermatologic Clinics, 1996, 14, 4, 753

    CrossRef

  11. 11
    Wim J. Kleijer, Frits A. Beemer, Bart W. Boom, Intermittent hair loss in a child with PIBI(D)S syndrome and trichothiodystrophy with defective DNA repair-xeroderma pigmentosum group D, American Journal of Medical Genetics, 1994, 52, 2
  12. 12
    Errol C. Friedberg, Karla A. Henning, The conundrum of xeroderma pigmentosum — A rare disease with frequent complexities, Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis, 1993, 289, 1, 47

    CrossRef

  13. 13
    Joseph H. Hersh, Laura R. Klein, Margie R. Joyce, Maria K. Hordinsky, Michael Y. Tsai, Amy Pafler, Resa Hyzer, Robert H. Zax, Trichothiodystrophy and Associated Anomalies: A Variant of SIBIDS or New Symptom Complex?, Pediatric Dermatology, 1993, 10, 2
  14. 14
    Catherine McCuaig, Danielle Marcoux, James E. Rasmussen, Mary M. Werner, Norman E. Gentner, Trichothiodystrophy associated with photosensitivity, gonadal failure, and striking osteosclerosis, Journal of the American Academy of Dermatology, 1993, 28, 5, 820

    CrossRef

  15. 15
    Boris G. Kousseff, Trichothiodystrophy and ichthyosis as diagnostic signs, American Journal of Medical Genetics, 1991, 40, 1