SEARCH

SEARCH BY CITATION

Cited in:

CrossRef

This article has been cited by:

  1. 1
    Weining Lu, Kevin T. Bush, Sanjay K. Nigam, Kidney Development, Disease, Repair and Regeneration, 2016,

    CrossRef

  2. 2
    Benjamin D. Solomon, Kelly A. Bear, Virginia Kimonis, Annelies de Klein, Daryl A. Scott, Charles Shaw-Smith, Dick Tibboel, Heiko Reutter, Philip F. Giampietro, Clinical geneticists' views of VACTERL/VATER association, American Journal of Medical Genetics Part A, 2012, 158A, 12
  3. 3
    Lawrence Copelovitch, Bernard S. Kaplan, Avery's Diseases of the Newborn, 2012,

    CrossRef

  4. 4
    Feng Cheng, Xin Ke, Ming Lv, Fan Zhang, Chaohua Li, Xianglong Zhang, Yinan Zhang, Xiangjun Zhao, Xingwu Wang, Bo Liu, Jinxiang Han, Yan Li, Changqing Zeng, Sheng Li, A novel frame-shift mutation of GLI3 causes non-syndromic and complex digital anomalies in a Chinese family, Clinica Chimica Acta, 2011, 412, 11-12, 1012

    CrossRef

  5. 5
    Erin Mundt, Michael D. Bates, Genetics of Hirschsprung disease and anorectal malformations, Seminars in Pediatric Surgery, 2010, 19, 2, 107

    CrossRef

  6. 6
    Jennifer J. Johnston, Julie C. Sapp, Joyce T. Turner, David Amor, Salim Aftimos, Kyrieckos A. Aleck, Maureen Bocian, Joann N. Bodurtha, Gerald F. Cox, Cynthia J. Curry, Ruth Day, Dian Donnai, Michael Field, Ikuma Fujiwara, Michael Gabbett, Moran Gal, John M. Graham, Peter Hedera, Raoul C.M. Hennekam, Joseph H. Hersh, Robert J. Hopkin, Hülya Kayserili, Alexa M.J. Kidd, Virginia Kimonis, Angela E. Lin, Sally Ann Lynch, Melissa Maisenbacher, Sahar Mansour, Julie McGaughran, Lakshmi Mehta, Helen Murphy, Margarita Raygada, Nathaniel H. Robin, Alan F. Rope, Kenneth N. Rosenbaum, G. Bradley Schaefer, Amy Shealy, Wendy Smith, Maria Soller, Annmarie Sommer, Heather J. Stalker, Bernhard Steiner, Mark J. Stephan, David Tilstra, Susan Tomkins, Pamela Trapane, Anne Chun-Hui Tsai, Margot I. Van Allen, Pradeep C. Vasudevan, Bernhard Zabel, Janice Zunich, Graeme C.M. Black, Leslie G. Biesecker, Molecular analysis expands the spectrum of phenotypes associated with GLI3 mutations, Human Mutation, 2010, 31, 10
  7. 7
    GEORGE HALEBLIAN, DAVID KRAKLAU, DUNCAN WILCOX, PATRICK DUFFY, PHILIP RANSLEY, IMRAN MUSHTAQ, Y-type urethral duplication in the male, BJU International, 2006, 97, 3
  8. 8
    LG Biesecker, Mapping phenotypes to language: a proposal to organize and standardize the clinical descriptions of malformations, Clinical Genetics, 2005, 68, 4
  9. 9
    Jennifer J. Johnston, Isabelle Olivos-Glander, Christina Killoran, Emma Elson, Joyce T. Turner, Kathryn F. Peters, Margaret H. Abbott, David J. Aughton, Arthur S. Aylsworth, Michael J. Bamshad, Carol Booth, Cynthia J. Curry, Albert David, Mary Beth Dinulos, David B. Flannery, Michelle A. Fox, John M. Graham, Dorothy K. Grange, Alan E. Guttmacher, Mark C. Hannibal, Wolfram Henn, RaoulC.M. Hennekam, Lewis B. Holmes, H. Eugene Hoyme, Kathleen A. Leppig, Angela E. Lin, Patrick MacLeod, David K. Manchester, Carlo Marcelis, Laura Mazzanti, Emma McCann, Marie T. McDonald, Nancy J. Mendelsohn, John B. Moeschler, Billur Moghaddam, Giovanni Neri, Ruth Newbury-Ecob, Roberta A. Pagon, John A. Phillips III, Laurie S. Sadler, Joan M. Stoler, David Tilstra, Catherine M. Walsh Vockley, Elaine H. Zackai, Touran M. Zadeh, Louise Brueton, Graeme Charles M. Black, Leslie G. Biesecker, Molecular and Clinical Analyses of Greig Cephalopolysyndactyly and Pallister-Hall Syndromes: Robust Phenotype Prediction from the Type and Position of GLI3 Mutations, The American Journal of Human Genetics, 2005, 76, 4, 609

    CrossRef

  10. 10
    T. Roscioli, D. Kennedy, J. Cui, B. Fonseca, G.F. Watson, J. Pereira, Y-G. Xie, D. Mowat, Pallister–Hall syndrome: Unreported skeletal features of a GLI3 mutation, American Journal of Medical Genetics Part A, 2005, 136A, 4
  11. 11
    Han G. Brunner, Marc A. van Driel, Opinion: From syndrome families to functional genomics, Nature Reviews Genetics, 2004, 5, 7, 545

    CrossRef

  12. 12
    Év Morava, Marta Czakó, Judit Kárteszi, Beatrix Cser, Karen Weissbecker, Karoly Méhes, Ulnar/fibular ray defect and brachydactyly in a family: a possible new autosomal dominant syndrome, Clinical Dysmorphology, 2003, 12, 3, 161

    CrossRef

  13. 13
    ??va Morava, Marta Czak??, Judit K??rteszi, Beatrix Cser, Karen Weissbecker, Karoly M??hes, Ulnar/fibular ray defect and brachydactyly in a family: a possible new autosomal dominant syndrome, Clinical Dysmorphology, 2003, 12, 3, 161

    CrossRef

  14. 14
    Leslie G. Biesecker, Polydactyly: How many disorders and how many genes?, American Journal of Medical Genetics, 2002, 112, 3
  15. 15
    JH Kim, PCW Kim, C-C Hui, The VACTERL association: lessons from the Sonic hedgehog pathway, Clinical Genetics, 2001, 59, 5
  16. 16
    Leslie G. Biesecker, Pallister-Hall Syndrome and Greig Cephalopolysyndactyly Syndrome,
  17. 17
    Bryan D. Hall, VATER Association, Management of Genetic Syndromes,
  18. 18
    Bryan D. Hall, Vater/Vacterl Association,