SEARCH

SEARCH BY CITATION

Cited in:

CrossRef

This article has been cited by:

  1. 1
    Alexa Sadier, Laurent Viriot, Sophie Pantalacci, Vincent Laudet, The ectodysplasin pathway: from diseases to adaptations, Trends in Genetics, 2014, 30, 1, 24

    CrossRef

  2. 2
    Jasna Dietz, Thomas Kaercher, Anne-Theres Schneider, Theodor Zimmermann, Kenneth Huttner, Ramsey Johnson, Holm Schneider, Early respiratory and ocular involvement in X-linked hypohidrotic ectodermal dysplasia, European Journal of Pediatrics, 2013, 172, 8, 1023

    CrossRef

  3. 3
    Marijn Créton, Marie-José Boogaard, Thomas Maal, Luc Verhamme, Willem Fennis, Carine Carels, Anne Marie Kuijpers-Jagtman, Marco Cune, Three-dimensional analysis of tooth dimensions in the MSX1-missense mutation, Clinical Oral Investigations, 2013, 17, 5, 1437

    CrossRef

  4. 4
    M. Pavlovsky, D. Fuchs-Telem, J. Nousbeck, O. Sarig, E. Sprecher, Molecular evidence for the role of X-chromosome inactivation in linear presentation of X-linked hypohidrotic ectodermal dysplasia, Clinical and Experimental Dermatology, 2012, 37, 2
  5. 5
    Wei Yin, XiaoQian Ye, Zhuan Bian, Phenotypic findings in Chinese families with X-linked hypohydrotic ectodermal dysplasia, Archives of Oral Biology, 2012, 57, 10, 1418

    CrossRef

  6. 6
    Mark M. Tran, Bernard A. Cohen, Avery's Diseases of the Newborn, 2012,

    CrossRef

  7. 7
    Jin Zhang, Dong Han, Shujuan Song, Ying Wang, Hongshan Zhao, Shaoxia Pan, Baojing Bai, Hailan Feng, Correlation between the phenotypes and genotypes of X-linked hypohidrotic ectodermal dysplasia and non-syndromic hypodontia caused by ectodysplasin-A mutations, European Journal of Medical Genetics, 2011, 54, 4, e377

    CrossRef

  8. 8
    V Desai, A Donsante, KJ Swoboda, M Martensen, J Thompson, SG Kaler, Favorably skewed X-inactivation accounts for neurological sparing in female carriers of Menkes disease, Clinical Genetics, 2011, 79, 2
  9. You have open access to this content9
    Ruben Agrelo, Anton Wutz, ConteXt of change—X inactivation and disease, EMBO Molecular Medicine, 2010, 2, 1
  10. 10
    Mia Færch, Thomas J. corydon, Søren Rittig, Jane H. Christensen, Jens Michael Hertz, Johan Jendle, Skewed X-chromosome inactivation causing diagnostic misinterpretation in congenital nephrogenic diabetes insipidus, Scandinavian Journal of Urology and Nephrology, 2010, 44, 5, 324

    CrossRef

  11. 11
    F Clauss, N Chassaing, A Smahi, MC Vincent, P Calvas, M Molla, H Lesot, Y Alembik, S Hadj-Rabia, C Bodemer, MC Manière, M Schmittbuhl, X-linked and autosomal recessive Hypohidrotic Ectodermal Dysplasia: genotypic-dental phenotypic findings, Clinical Genetics, 2010, 78, 3
  12. You have free access to this content12
    Gabriele I. Mues, Rachel Griggs, Andrew J. Hartung, Greg Whelan, Lyle G. Best, Anand K. Srivastava, Rena D'Souza, From ectodermal dysplasia to selective tooth agenesis, American Journal of Medical Genetics Part A, 2009, 149A, 9
  13. 13
    S. Stagi, E. Lapi, I. Sani, G. Bindi, M.R. Quaranta, R. Salti, F. Chiarelli, Growth Hormone Neurosecretory Dysfunction in a Boy with Hypohidrotic/Anhidrotic Ectodermal Dysplasie: Definition of Short Stature, Molecular Characterization and Long-term hGH Replacement Treatment to Final Height, Journal of Pediatric Endocrinology and Metabolism, 2009, 22, 9

    CrossRef

  14. 14
    Gunadi, Kenji Miura, Mika Ohta, Aki Sugano, Myeong Jin Lee, Yumi Sato, Akiko Matsunaga, Kazuhiro Hayashi, Tatsuya Horikawa, Kazunori Miki, Mari Wataya-Kaneda, Ichiro Katayama, Chikako Nishigori, Masafumi Matsuo, Yutaka Takaoka, Hisahide Nishio, Two Novel Mutations in the ED1 Gene in Japanese Families With X-Linked Hypohidrotic Ectodermal Dysplasia, Pediatric Research, 2009, 65, 4, 453

    CrossRef

  15. 15
    Karen Helene Ørstavik, X chromosome inactivation in clinical practice, Human Genetics, 2009, 126, 3, 363

    CrossRef