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Cornelia de Lange syndrome: Clinical review, diagnostic and scoring systems, and anticipatory guidance Am J Med Genet Part A 143A:1287–1296

  1. Antonie D. Kline1,*,
  2. Ian D. Krantz2,
  3. Annemarie Sommer3,
  4. Mark Kliewer4,
  5. Laird G. Jackson2,5,
  6. David R. FitzPatrick6,
  7. Alex V. Levin7,
  8. Angelo Selicorni8

Article first published online: 24 SEP 2008

DOI: 10.1002/ajmg.a.32469

Issue

American Journal of Medical Genetics Part A

American Journal of Medical Genetics Part A

Volume 146A, Issue 20, page 2713, 15 October 2008

Additional Information

How to Cite

Kline, A. D., Krantz, I. D., Sommer, A., Kliewer, M., Jackson, L. G., FitzPatrick, D. R., Levin, A. V. and Selicorni, A. (2008), Cornelia de Lange syndrome: Clinical review, diagnostic and scoring systems, and anticipatory guidance Am J Med Genet Part A 143A:1287–1296. Am. J. Med. Genet., 146A: 2713. doi: 10.1002/ajmg.a.32469

Author Information

  1. 1

    Harvey Institute for Human, Genetics, Department of Pediatrics, Greater Baltimore Medical Center, Baltimore, MD

  2. 2

    Division of Human Genetics and Molecular Biology, The Children's Hospital of Philadelphia, University of Pennsylvania, Philadelphia, PA

  3. 3

    Department of Human Genetics, Columbus Children's Hospital, Columbus, OH

  4. 4

    Department of Radiology, University of Wisconsin, Madison, WS

  5. 5

    Division of Medical Genetics, Drexel University, Philadelphia, PA

  6. 6

    Medical Research Council Human Genetics Unit, Edinburgh, United Kingdom

  7. 7

    Department of Ophthalmology and Vision Sciences, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada

  8. 8

    Clinical Genetics, Department of Pediatrics, Milan, Italy.

*Harvey Institute for Human Genetics, Greater Baltimore Medical Center, 6701 N. Charles St., Suite 2326, Baltimore, MD 21204.

Publication History

  1. Issue published online: 24 SEP 2008
  2. Article first published online: 24 SEP 2008

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