SEARCH

SEARCH BY CITATION

Cited in:

CrossRef

This article has been cited by:

  1. 1
    Ellen M. Chung, Richard M. Conran, Jason W. Schroeder, Ivan R. Rohena-Quinquilla, Veronica J. Rooks, From the Radiologic Pathology Archives: Pediatric Polycystic Kidney Disease and Other Ciliopathies: Radiologic-Pathologic Correlation, RadioGraphics, 2014, 34, 1, 155

    CrossRef

  2. 2
    Jan Halbritter, Albane A. Bizet, Miriam Schmidts, Jonathan D. Porath, Daniela A. Braun, Heon Yung Gee, Aideen M. McInerney-Leo, Pauline Krug, Emilie Filhol, Erica E. Davis, Rannar Airik, Peter G. Czarnecki, Anna M. Lehman, Peter Trnka, Patrick Nitschké, Christine Bole-Feysot, Markus Schueler, Bertrand Knebelmann, Stéphane Burtey, Attila J. Szabó, Kálmán Tory, Paul J. Leo, Brooke Gardiner, Fiona A. McKenzie, Andreas Zankl, Matthew A. Brown, Jane L. Hartley, Eamonn R. Maher, Chunmei Li, Michel R. Leroux, Peter J. Scambler, Shing H. Zhan, Steven J. Jones, Hülya Kayserili, Beyhan Tuysuz, Khemchand N. Moorani, Alexandru Constantinescu, Ian D. Krantz, Bernard S. Kaplan, Jagesh V. Shah, Toby W. Hurd, Dan Doherty, Nicholas Katsanis, Emma L. Duncan, Edgar A. Otto, Philip L. Beales, Hannah M. Mitchison, Sophie Saunier, Friedhelm Hildebrandt, Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans, The American Journal of Human Genetics, 2013, 93, 5, 915

    CrossRef

  3. 3
    Miriam Schmidts, Julia Vodopiutz, Sonia Christou-Savina, Claudio R. Cortés, Aideen M. McInerney-Leo, Richard D. Emes, Heleen H. Arts, Beyhan Tüysüz, Jason D’Silva, Paul J. Leo, Tom C. Giles, Machteld M. Oud, Jessica A. Harris, Marije Koopmans, Mhairi Marshall, Nursel Elçioglu, Alma Kuechler, Detlef Bockenhauer, Anthony T. Moore, Louise C. Wilson, Andreas R. Janecke, Matthew E. Hurles, Warren Emmet, Brooke Gardiner, Berthold Streubel, Belinda Dopita, Andreas Zankl, Hülya Kayserili, Peter J. Scambler, Matthew A. Brown, Philip L. Beales, Carol Wicking, Emma L. Duncan, Hannah M. Mitchison, Mutations in the Gene Encoding IFT Dynein Complex Component WDR34 Cause Jeune Asphyxiating Thoracic Dystrophy, The American Journal of Human Genetics, 2013, 93, 5, 932

    CrossRef

  4. 4
    Andrew Bush, Claire Hogg, Primary ciliary dyskinesia: recent advances in epidemiology, diagnosis, management and relationship with the expanding spectrum of ciliopathy, Expert Review of Respiratory Medicine, 2012, 6, 6, 663

    CrossRef

  5. 5
    Kim M. Keppler-Noreuil, Margaret P. Adam, Judy Welch, Ann Muilenburg, Marcia C. Willing, Clinical insights gained from eight new cases and review of reported cases with Jeune syndrome (asphyxiating thoracic dystrophy), American Journal of Medical Genetics Part A, 2011, 155, 5
  6. 6
    Matthew J. O’Connor, Nicholas L. Rider, R. Thomas Collins, Brian D. Hanna, D. Holmes Morton, Kevin A. Strauss, Contemporary management of congenital malformations of the heart in infants with Ellis – van Creveld syndrome: a report of nine cases, Cardiology in the Young, 2011, 21, 02, 145

    CrossRef

  7. 7
    A.M. Lehman, P. Eydoux, D. Doherty, I.A. Glass, D. Chitayat, B.Y.H. Chung, S. Langlois, S.L. Yong, R.B. Lowry, F. Hildebrandt, P. Trnka, Co-occurrence of Joubert syndrome and Jeune asphyxiating thoracic dystrophy, American Journal of Medical Genetics Part A, 2010, 152A, 6
  8. 8
    H. Aloulou, H. Turki, I. Chabchoub, L. Ben Mansour, T. Kammoun, M. Hachicha, Dystrophie thoracique de Jeune compliquée d’atteinte rénale : étude de deux observations, Journal de Pédiatrie et de Puériculture, 2010, 23, 3, 141

    CrossRef