SEARCH

SEARCH BY CITATION

Cited in:

CrossRef

This article has been cited by:

  1. 1
    Anas M. Alazami, Mohammed Zain Seidahmed, Fatema Alzahrani, Adam O. Mohammed, Fowzan S. Alkuraya, Novel IFT122 mutation associated with impaired ciliogenesis and cranioectodermal dysplasia, Molecular Genetics & Genomic Medicine, 2014, 2, 2
  2. 2
    Heleen H. Arts, Nine V. A. M. Knoers, Current insights into renal ciliopathies: what can genetics teach us?, Pediatric Nephrology, 2013, 28, 6, 863

    CrossRef

  3. You have free access to this content3
    Angela E. Lin, Avram Z. Traum, Inderneel Sahai, Kim Keppler-Noreuil, Mary K. Kukolich, Margaret P. Adam, Sjirk J. Westra, Heleen H. Arts, Sensenbrenner syndrome (Cranioectodermal dysplasia): Clinical and molecular analyses of 39 patients including two new patients, American Journal of Medical Genetics Part A, 2013, 161, 11
  4. 4
    Thomas W. Ferkol, Margaret W. Leigh, Ciliopathies: The Central Role of Cilia in a Spectrum of Pediatric Disorders, The Journal of Pediatrics, 2012, 160, 3, 366

    CrossRef

  5. 5
    Carsten Bergmann, Educational paper, European Journal of Pediatrics, 2012, 171, 9, 1285

    CrossRef

  6. 6
    Carlos A. Bacino, Shweta U. Dhar, Nicola Brunetti-Pierri, Brendan Lee, Penelope E. Bonnen, WDR35 mutation in siblings with Sensenbrenner syndrome: A ciliopathy with variable phenotype, American Journal of Medical Genetics Part A, 2012, 158A, 11
  7. You have free access to this content7
    Norann A. Zaghloul, Samantha A. Brugmann, The emerging face of primary cilia, genesis, 2011, 49, 4
  8. 8
    Joanna Walczak-Sztulpa, Jonathan Eggenschwiler, Daniel Osborn, Desmond A. Brown, Francesco Emma, Claus Klingenberg, Raoul C. Hennekam, Giuliano Torre, Masoud Garshasbi, Andreas Tzschach, Malgorzata Szczepanska, Marian Krawczynski, Jacek Zachwieja, Danuta Zwolinska, Philip L. Beales, Hans-Hilger Ropers, Anna Latos-Bielenska, Andreas W. Kuss, Cranioectodermal Dysplasia, Sensenbrenner Syndrome, Is a Ciliopathy Caused by Mutations in the IFT122 Gene, The American Journal of Human Genetics, 2010, 86, 6, 949

    CrossRef

  9. You have free access to this content9
    Samantha A. Brugmann, Dwight R. Cordero, Jill A. Helms, Craniofacial ciliopathies: A new classification for craniofacial disorders, American Journal of Medical Genetics Part A, 2010, 152A, 12