Research Article

Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia†

  1. Margaret J. Wat1,
  2. Oleg A. Shchelochkov1,
  3. Ashley M. Holder2,
  4. Amy M. Breman1,
  5. Aditi Dagli3,
  6. Carlos Bacino1,
  7. Fernando Scaglia1,
  8. Roberto T. Zori3,
  9. Sau Wai Cheung1,
  10. Daryl A. Scott1,
  11. Sung-Hae Lee Kang1,*

Article first published online: 15 JUL 2009

DOI: 10.1002/ajmg.a.32896

Issue

American Journal of Medical Genetics Part A

American Journal of Medical Genetics Part A

Volume 149A, Issue 8, pages 1661–1677, August 2009

Additional Information

How to Cite

Wat, M. J., Shchelochkov, O. A., Holder, A. M., Breman, A. M., Dagli, A., Bacino, C., Scaglia, F., Zori, R. T., Cheung, S. W., Scott, D. A. and Kang, S.-H. L. (2009), Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia. Am. J. Med. Genet., 149A: 1661–1677. doi: 10.1002/ajmg.a.32896

Author Information

  1. 1

    Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas

  2. 2

    Department of Surgery, Washington University School of Medicine, Saint Louis, Missouri

  3. 3

    Department of Pediatrics, University of Florida, Gainesville, Florida

*Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX.

  1. †

    How to cite this article: Wat MJ, Shchelochkov OA, Holder AM, Breman AM, Dagli A, Bacino C, Scaglia F, Zori RT, Cheung SW, Scott DA, Kang S-HL. 2009. Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia. Am J Med Genet Part A 149A:1661–1677.

Publication History

  1. Issue published online: 23 JUL 2009
  2. Article first published online: 15 JUL 2009
  3. Manuscript Accepted: 2 APR 2009
  4. Manuscript Received: 22 DEC 2008

Funded by

  • NIH. Grant Number: HD-050583

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