Birth Defects Research Part A: Clinical and Molecular Teratology

Cover image for Vol. 97 Issue 12

December 2013

Volume 97, Issue 12

Pages 759–815

  1. Original Research Articles

    1. Top of page
    2. Original Research Articles
    3. Brief Reports
    4. Original Research Articles
    5. Brief Reports
    6. Original Research Articles
    7. Brief Reports
    1. Candidate gene association study implicates p63 in the etiology of nonsyndromic bladder-exstrophy-epispadias complex (pages 759–763)

      Lihong Qi, Mei Wang, Garima Yagnik, Manuel Mattheisen, John P. Gearhart, Yegappan lakshmanan, Anne-Karolin Ebert, Wolfgang Rösch, Michael Ludwig, Markus Draaken, Heiko Reutter and Simeon A. Boyadjiev

      Version of Record online: 2 AUG 2013 | DOI: 10.1002/bdra.23161

  2. Brief Reports

    1. Top of page
    2. Original Research Articles
    3. Brief Reports
    4. Original Research Articles
    5. Brief Reports
    6. Original Research Articles
    7. Brief Reports
    1. Novel mutations in ADAMTSL2 gene underlying geleophysic dysplasia in families from United Arab Emirates (pages 764–769)

      Salma Ben-Salem, Jozef Hertecant, Aisha M. Al-Shamsi, Bassam R. Ali and Lihadh Al-Gazali

      Version of Record online: 6 SEP 2013 | DOI: 10.1002/bdra.23170

  3. Original Research Articles

    1. Top of page
    2. Original Research Articles
    3. Brief Reports
    4. Original Research Articles
    5. Brief Reports
    6. Original Research Articles
    7. Brief Reports
    1. Prenatal diagnosis of femoral–facial syndrome: Report of two cases (pages 770–773)

      Emil Silvas, Françoise Rypens, Mubina Jovanovic, Anne-Lise Delezoide and Natalie Patey

      Version of Record online: 19 NOV 2013 | DOI: 10.1002/bdra.23201

    2. Mandibulofacial dysostosis (Treacher-Collins syndrome) in the fetus: Novel association with pectus carinatum in a molecularly confirmed case and review of the fetal phenotype (pages 774–780)

      Anastasia E. Konstantinidou, Jason Tasoulas, Georgios Kallipolitis, Spyros Gasparatos, Voula Velissariou and Helen Paraskevakou

      Version of Record online: 29 NOV 2013 | DOI: 10.1002/bdra.23202

  4. Brief Reports

    1. Top of page
    2. Original Research Articles
    3. Brief Reports
    4. Original Research Articles
    5. Brief Reports
    6. Original Research Articles
    7. Brief Reports
    1. Patient with disorganization syndrome: Surgical procedures, Pathology, and potential causes (pages 781–785)

      Oscar Girón Vallejo, María del Carmen Benítez Sánchez, Cesar Salcedo Cánovas, Joanna Díez Ontiveros, José Ignacio Ruiz Jiménez, Eva Bermejo-Sánchez and María Luisa Martínez-Frías

      Version of Record online: 4 DEC 2013 | DOI: 10.1002/bdra.23203

  5. Original Research Articles

    1. Top of page
    2. Original Research Articles
    3. Brief Reports
    4. Original Research Articles
    5. Brief Reports
    6. Original Research Articles
    7. Brief Reports
    1. Second study on the recurrence risk of isolated esophageal atresia with or without trachea-esophageal fistula among first-degree relatives: No evidence for increased risk of recurrence of EA/TEF or for malformations of the VATER/VACTERL association spectrum (pages 786–791)

      Vera Choinitzki, Nadine Zwink, Enrika Bartels, Friederike Baudisch, Thomas M. Boemers, Alice Hölscher, Salmai Turial, Haitham Bachour, Andreas Heydweiller, Ralf Kurz, Peter Bartmann, Markus Pauly, Ulrike Brokmeier, Andreas Leutner, Markus M. Nöthen, Johannes Schumacher, Ekkehart Jenetzky and Heiko Reutter

      Version of Record online: 5 DEC 2013 | DOI: 10.1002/bdra.23205

    2. Analysis of cardiac anomalies in VACTERL association (pages 792–797)

      Bridget K. Cunningham, Donald W. Hadley, Hwaida Hannoush, Andrew C. Meltzer, Nickie Niforatos, Daniel Pineda-Alvarez, Vandana Sachdev, Nicole Warren-Mora and Benjamin D. Solomon

      Version of Record online: 17 DEC 2013 | DOI: 10.1002/bdra.23211

    3. Genetic Basis of Congenital Upper Limb Anomalies: Analysis of 487 Cases of a Specialized Clinic (pages 798–805)

      Diana Carli, Tracy Fairplay, Paola Ferrari, Silvana Sartini, Mario Lando, Lorenzo Garagnani, Giovanni Luigi Di Gennaro, Luciana Di Pancrazio, Giorgia Bianconi, Amira Elmakky, Sergio Bernasconi, Antonio Landi and Antonio Percesepe

      Version of Record online: 17 DEC 2013 | DOI: 10.1002/bdra.23212

  6. Brief Reports

    1. Top of page
    2. Original Research Articles
    3. Brief Reports
    4. Original Research Articles
    5. Brief Reports
    6. Original Research Articles
    7. Brief Reports
    1. Prenatal ultrasound findings observed in the Wolf-hirschhorn syndrome: Data from the registry of congenital malformations in auvergne (pages 806–811)

      Anne Debost-Legrand, Carole Goumy, Hélène Laurichesse-Delmas, Pierre Déchelotte, Anne-Marie Beaufrère, Didier Lémery, Christine Francannet and Denis Gallot

      Version of Record online: 6 NOV 2013 | DOI: 10.1002/bdra.23194

    2. Tetrasomy 13q32.2qter due to an apparent inverted duplicated neocentric marker chromosome in an infant with hemangiomas, failure to thrive, laryngomalacia, and tethered cord (pages 812–815)

      Jinglan Liu, Reena Jethva, Michael T. Del Vecchio, John E. Hauptman, Judy M. Pascasio and Jean-Pierre de Chadarévian

      Version of Record online: 12 NOV 2013 | DOI: 10.1002/bdra.23197

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