SEARCH

SEARCH BY CITATION

Cited in:

CrossRef

This article has been cited by:

  1. 1
    Earl Silverman, Jill Buyon, Edgar Jaeggi, Textbook of Pediatric Rheumatology, 2016,

    CrossRef

  2. 2
    Irena Vrečar, Gorazd Rudolf, Borut Peterlin, Luca Lovrecic, Brachytelephalangic chondrodysplasia punctata caused by new small hemizygous deletion in a boy presenting with hearing loss, Molecular Cytogenetics, 2015, 8, 1

    CrossRef

  3. 3
    Natalia Marin Huarte, Fernando Santos-Simarro, Ignacio Pastor Abascal, Sixto García-Miñaur, Felix Omeñaca, Chondrodysplasia punctata associated with maternal Sjögren syndrome, American Journal of Medical Genetics Part A, 2014, 164, 6
  4. 4
    Claudia Matos-Miranda, Graeme Nimmo, Bradley Williams, Carolyn Tysoe, Martina Owens, Sherri Bale, Nancy Braverman, A prospective study of brachytelephalangic chondrodysplasia punctata: identification of arylsulfatase E mutations, functional analysis of novel missense alleles, and determination of potential phenocopies, Genetics in Medicine, 2013, 15, 8, 650

    CrossRef

  5. 5
    Anna Dobrzanska, Clinical and radiological pictures of two newborn babies with manifestations of chondrodysplasia punctata and review of available literature., Polish Journal of Radiology, 2013, 78, 2, 57

    CrossRef

  6. 6
    Helga V. Toriello, Miriam Erick, Jean-Luc Alessandri, Diana Bailey, Nicola Brunetti-Pierri, Helen Cox, Alan Fryer, Denise Marty, Charles McCurdy, John B. Mulliken, Helen Murphy, Joseph Omlor, Richard M. Pauli, Judith D. Ranells, Amarillis Sanchez-Valle, Ana Tobiasz, Lionel Van Maldergem, Angela E. Lin, Maternal vitamin K deficient embryopathy: Association with hyperemesis gravidarum and Crohn disease, American Journal of Medical Genetics Part A, 2013, 161, 3
  7. 7
    E. Colin, R. Touraine, J. M. Levaillant, L. Pasquier, F. Boussion, M. Ferry, A. Guichet, M. Barth, A. Mercier, M. Gérard-Blanluet, S. Odent, D. Bonneau, Binder phenotype in mothers affected with autoimmune disorders, The Journal of Maternal-Fetal & Neonatal Medicine, 2012, 25, 8, 1413

    CrossRef

  8. 8
    M. Cassina, D. L. Johnson, L. K. Robinson, S. R. Braddock, R. Xu, J. L. Jimenez, N. Mirrasoul, E. Salas, Y. J. Luo, K. L. Jones, C. D. Chambers, Pregnancy outcome in women exposed to leflunomide before or during pregnancy, Arthritis & Rheumatism, 2012, 64, 7
  9. 9
    Thipwimol Tim-aroon, Suphaneewan Jaovisidha, Duangrurdee Wattanasirichaigoon, A new case of maternal lupus-associated chondrodysplasia punctata with extensive spinal anomalies, American Journal of Medical Genetics Part A, 2011, 155, 6
  10. 10
    Helen Wainwright, Peter Beighton, Lethal epiphyseal stippling in the foetus and neonate; pathological implications, Virchows Archiv, 2010, 456, 3, 301

    CrossRef

  11. 11
    Steffan W. Schulz, Michael Bober, Caitlyn Johnson, Nancy Braverman, Sergio A. Jimenez, Maternal Mixed Connective Tissue Disease and Offspring with Chondrodysplasia Punctata, Seminars in Arthritis and Rheumatism, 2010, 39, 5, 410

    CrossRef

  12. 12
    E. Silverman, E. Jaeggi, Non-Cardiac Manifestations of Neonatal Lupus Erythematosus, Scandinavian Journal of Immunology, 2010, 72, 3
  13. 13
    David Chitayat, Sarah Keating, Dina J. Zand, Teresa Costa, Elaine H. Zackai, Earl Silverman, George Tiller, Sheila Unger, Stephen Miller, John Kingdom, Ants Toi, Cynthia J.R. Curry, Chondrodysplasia punctata associated with maternal autoimmune diseases: Expanding the spectrum from systemic lupus erythematosus (SLE) to mixed connective tissue disease (MCTD) and scleroderma report of eight cases, American Journal of Medical Genetics Part A, 2008, 146A, 23
  14. 14
    Melita D. Irving, Lyn S. Chitty, Sahar Mansour, Christine M. Hall, Chondrodysplasia punctata: a clinical diagnostic and radiological review, Clinical Dysmorphology, 2008, 17, 4, 229

    CrossRef

  15. 15
    Michelle Nino, Claudia Matos-Miranda, Momoe Maeda, Li Chen, Judith Allanson, Christine Armour, Carol Greene, Majeeda Kamaluddeen, Debra Rita, Livija Medne, Elaine Zackai, Sahar Mansour, Andrea Superti-Furga, Amy Lewanda, Michael Bober, Kenneth Rosenbaum, Nancy Braverman, Clinical and molecular analysis of arylsulfatase E in patients with brachytelephalangic chondrodysplasia punctata, American Journal of Medical Genetics Part A, 2008, 146A, 8
  16. 16
    Rie Honda, Takashi Ichiyama, Shinji Maeba, Shinpei Sunagawa, Susumu Furukawa, Male siblings with tibia-metacarpal type of chondrodysplasia punctata without maternal factors, Brain and Development, 2008, 30, 4, 301

    CrossRef

  17. 17
    Nicola Brunetti-Pierri, Jill V. Hunter, Cornelius F. Boerkoel, Gray matter heterotopias and brachytelephalangic chondrodysplasia punctata: A complication of hyperemesis gravidarum induced vitamin K deficiency?, American Journal of Medical Genetics Part A, 2007, 143A, 2
  18. 18
    Yorck Hellenbroich, Karl-Heinz Grzeschik, Martin Krapp, Tiantom Jarutat, Christa Lehrmann-Petersen, Karin Buiting, Gabriele Gillessen-Kaesbach, Reduced penetrance in a family with X-linked dominant chondrodysplasia punctata, European Journal of Medical Genetics, 2007, 50, 5, 392

    CrossRef

  19. 19
    Shalini Umranikar, Phyllis Glanc, Sheila Unger, Sarah Keating, Katherine Fong, Christopher D Trevors, Diane Myles-Reid, David Chitayat, X-Linked dominant chondrodysplasia punctata: prenatal diagnosis and autopsy findings, Prenatal Diagnosis, 2006, 26, 13