Birth Defects Research Part A: Clinical and Molecular Teratology

Cover image for Vol. 100 Issue 4

April 2014

Volume 100, Issue 4

Pages I–IV, 247–318

  1. Issue Information

    1. Top of page
    2. Issue Information
    3. Original Research Articles
    4. Case Report
    5. Brief Report
    6. Original Research Articles
    7. Brief Report
    1. You have free access to this content
      Issue information (pages I–IV)

      Article first published online: 22 APR 2014 | DOI: 10.1002/bdra.23183

  2. Original Research Articles

    1. Top of page
    2. Issue Information
    3. Original Research Articles
    4. Case Report
    5. Brief Report
    6. Original Research Articles
    7. Brief Report
    1. Mortality in babies with achondroplasia: Revisited (pages 247–249)

      Kristen Simmons, S. Shahrukh Hashmi, Angela Scheuerle, Mark Canfield and Jacqueline T. Hecht

      Article first published online: 12 FEB 2014 | DOI: 10.1002/bdra.23210

    2. Quantification of facial skeletal shape variation in fibroblast growth factor receptor-related craniosynostosis syndromes (pages 250–259)

      Yann Heuzé, Neus Martínez-Abadías, Jennifer M. Stella, Eric Arnaud, Corinne Collet, Gemma García Fructuoso, Mariana Alamar, Lun-Jou Lo, Simeon A. Boyadjiev, Federico Di Rocco and Joan T. Richtsmeier

      Article first published online: 27 FEB 2014 | DOI: 10.1002/bdra.23228

    3. Seasonality of congenital anomalies in Europe (pages 260–269)

      Johannes Michiel Luteijn, Helen Dolk, Marie-Claude Addor, Larraitz Arriola, Ingeborg Barisic, Fabrizio Bianchi, Elisa Calzolari, Elizabeth Draper, Ester Garne, Miriam Gatt, Martin Haeusler, Babak Khoshnood, Bob McDonnell, Vera Nelen, Mary O'Mahony, Carmel Mullaney, Annette Queisser-Luft, Judith Rankin, David Tucker, Christine Verellen-Dumoulin, Hermien de Walle and Lyubov Yevtushok

      Article first published online: 17 MAR 2014 | DOI: 10.1002/bdra.23231

    4. Epidemiology of multiple congenital anomalies in Europe: A EUROCAT population-based registry study (pages 270–276)

      Elisa Calzolari, Ingeborg Barisic, Maria Loane, Joan Morris, Diana Wellesley, Helen Dolk, Marie-Claude Addor, Larraitz Arriola, Fabrizio Bianchi, Amanda J. Neville, Judith L.S. Budd, Kari Klungsoyr, Babak Khoshnood, Bob McDonnell, Vera Nelen, Annette Queisser-Luft, Judith Rankin, Anke Rissmann, Catherine Rounding, David Tucker, Christine Verellen-Dumoulin, Hermien de Walle and Ester Garne

      Article first published online: 11 APR 2014 | DOI: 10.1002/bdra.23240

  3. Case Report

    1. Top of page
    2. Issue Information
    3. Original Research Articles
    4. Case Report
    5. Brief Report
    6. Original Research Articles
    7. Brief Report
    1. Prenatal diagnosis of proximal partial trisomy 1q confirmed by comparative genomic hybridization array: Molecular cytogenetic analysis, fetal pathology and review of the literature (pages 284–293)

      Stavros Sifakis, Makarios Eleftheriades, Dimitra Kappou, Roberta Murru, Anastasia Konstantinidou, Sandro Orru, Monika Ziegler, Thomas Liehr, Emmanouil Manolakos and Ioannis Papoulidis

      Article first published online: 12 FEB 2014 | DOI: 10.1002/bdra.23213

  4. Brief Report

    1. Top of page
    2. Issue Information
    3. Original Research Articles
    4. Case Report
    5. Brief Report
    6. Original Research Articles
    7. Brief Report
  5. Original Research Articles

    1. Top of page
    2. Issue Information
    3. Original Research Articles
    4. Case Report
    5. Brief Report
    6. Original Research Articles
    7. Brief Report
    1. Rare nasal cleft in a patient with holoprosencephaly due to a mutation in the ZIC2 gene (pages 300–306)

      Clarice Pagani Savastano, Pricila Bernardi, Hector N. Seuánez, Miguel Ângelo Martins Moreira and Iêda Maria Orioli

      Article first published online: 12 FEB 2014 | DOI: 10.1002/bdra.23216

    2. Nonsyndromic cleft lip with or without cleft palate in arab populations: Genetic analysis of 15 risk loci in a novel case–control sample recruited in Yemen (pages 307–313)

      Khalid Ahmed Aldhorae, Anne C. Böhmer, Kerstin U. Ludwig, Ahlam Hibatulla Ali Esmail, Nezar Noor Al-Hebshi, Bärbel Lippke, Lina Gölz, Markus M. Nöthen, Nikolaos Daratsianos, Michael Knapp, Andreas Jäger and Elisabeth Mangold

      Article first published online: 13 MAR 2014 | DOI: 10.1002/bdra.23221

  6. Brief Report

    1. Top of page
    2. Issue Information
    3. Original Research Articles
    4. Case Report
    5. Brief Report
    6. Original Research Articles
    7. Brief Report
    1. Further evidence for FGF16 truncating mutations as the cause of X-linked recessive fusion of metacarpals 4 / 5 (pages 314–318)

      Aleksander Jamsheer, Robert Śmigiel, Aleksandra Jakubiak, Tomasz Zemojtel, Magdalena Socha, Peter N. Robinson and Stefan Mundlos

      Article first published online: 7 APR 2014 | DOI: 10.1002/bdra.23239

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