Birth Defects Research Part A: Clinical and Molecular Teratology

Cover image for Vol. 94 Issue 6

June 2012

Volume 94, Issue 6

Pages 417–498

  1. Review Articles

    1. Top of page
    2. Review Articles
    3. Original Articles
    4. Brief Reports
    5. Case Reports
    1. A systematic review to calculate background miscarriage rates using life table analysis (pages 417–423)

      Lyndsay Ammon Avalos, Claudia Galindo and De-Kun Li

      Version of Record online: 18 APR 2012 | DOI: 10.1002/bdra.23014

  2. Original Articles

    1. Top of page
    2. Review Articles
    3. Original Articles
    4. Brief Reports
    5. Case Reports
    1. Congenital heart defect case ascertainment by the Alberta Congenital Anomalies Surveillance System (pages 449–458)

      Tanya Bedard, R. Brian Lowry, Barbara Sibbald, Joyce R. Harder, Cynthia Trevenen, Vera Horobec and John D. Dyck

      Version of Record online: 4 APR 2012 | DOI: 10.1002/bdra.23007

    2. Investigation of SUMO pathway genes in the etiology of nonsyndromic cleft lip with or without cleft palate (pages 459–463)

      Eloisa Carta, Erwin Pauws, Anna C. Thomas, Konstantinos Mengrelis, Gudrun E. Moore, Melissa Lees and Philip Stanier

      Version of Record online: 10 APR 2012 | DOI: 10.1002/bdra.23008

    3. Region 8q24 is a susceptibility locus for nonsyndromic oral clefting in Brazil (pages 464–468)

      Luciano Abreu Brito, Lívia Máris Ribeiro Paranaiba, Camila Fernandes Silva Bassi, Cibele Masotti, Carolina Malcher, David Schlesinger, Katia Maria Rocha, Lucas Alvizi Cruz, Lígia Kobayashi Bárbara, Nivaldo Alonso, Diogo Franco, Elizabete Bagordakis, Hercílio Martelli Jr., Diogo Meyer, Ricardo D. Coletta and Maria Rita Passos-Bueno

      Version of Record online: 18 APR 2012 | DOI: 10.1002/bdra.23011

  3. Brief Reports

    1. Top of page
    2. Review Articles
    3. Original Articles
    4. Brief Reports
    5. Case Reports
    1. Hirschsprung's disease in the North of England: Prevalence, associated anomalies, and survival (pages 477–480)

      Kate E. Best, Svetlana V. Glinianaia, Mary Bythell and Judith Rankin

      Version of Record online: 18 APR 2012 | DOI: 10.1002/bdra.23016

    2. Combined effect of prenatal solvent exposure and GSTT1 or GSTM1 polymorphisms in the risk of birth defects (pages 481–485)

      Ronan Garlantézec, Cécile Chevrier, Isabelle Coiffec, Catherine Celebi and Sylvaine Cordier

      Version of Record online: 8 MAY 2012 | DOI: 10.1002/bdra.23018

    3. The CTIS Womb to Classroom Screening Program for the detection of agents with adverse effects on neuropsychological development (pages 486–493)

      Jane Adams, Patricia A. Janulewicz, Kelly Kao, Kenneth Lyons Jones and Christina Chambers

      Version of Record online: 21 APR 2012 | DOI: 10.1002/bdra.23009

  4. Case Reports

    1. Top of page
    2. Review Articles
    3. Original Articles
    4. Brief Reports
    5. Case Reports
    1. Familial Pelizaeus–Merzbacher disease caused by a 320.6-kb Xq22.2 duplication and the pathological findings of a male fetus (pages 494–498)

      Sophia Kitsiou-Tzeli, Anastasia Konstantinidou, Christalena Sofocleous, Konstantina Kosma, Areti Syrmou, Krinio Giannikou, Stavros Sifakis, Periklis Makrythanasis and Maria Tzetis

      Version of Record online: 18 APR 2012 | DOI: 10.1002/bdra.23015

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