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Clinical Report

A patient with a mild holoprosencephaly spectrum phenotype and heterotaxy and a 1.3 Mb deletion encompassing GLI2†

  1. Sietske H.G. Kevelam1,*,
  2. Jeske J.T. van Harssel1,
  3. Bert van der Zwaag1,
  4. Hubertus J.M. Smeets2,3,
  5. Aimee D.C. Paulussen2,3,
  6. Klaske D. Lichtenbelt1

Article first published online: 21 NOV 2011

DOI: 10.1002/ajmg.a.34350

Issue

American Journal of Medical Genetics Part A

American Journal of Medical Genetics Part A

Volume 158A, Issue 1, pages 166–173, January 2012

Additional Information

How to Cite

Kevelam, S. H.G., van Harssel, J. J.T., van der Zwaag, B., Smeets, H. J.M., Paulussen, A. D.C. and Lichtenbelt, K. D. (2012), A patient with a mild holoprosencephaly spectrum phenotype and heterotaxy and a 1.3 Mb deletion encompassing GLI2. Am. J. Med. Genet., 158A: 166–173. doi: 10.1002/ajmg.a.34350

Author Information

  1. 1

    Department of Medical Genetics, University Medical Center Utrecht, Utrecht, the Netherlands

  2. 2

    Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, the Netherlands

  3. 3

    School for Oncology and Developmental Biology (GROW), Maastricht University Medical Center, Maastricht, the Netherlands

*Division of Biomedical Genetics, Department of Medical Genetics, University Medical Center Utrecht, P.O. Box 85090, 3508 AB Utrecht, the Netherlands.

  1. †

    How to cite this article: Kevelam SHG, van Harssel JJT, van der Zwaag B, Smeets HJM, Paulussen ADC, Lichtenbelt KD. 2012. A patient with a mild holoprosencephaly spectrum phenotype and heterotaxy and a 1.3 Mb deletion encompassing GLI2. Am J Med Genet Part A 158A:166–173.

Publication History

  1. Issue published online: 19 DEC 2011
  2. Article first published online: 21 NOV 2011
  3. Manuscript Accepted: 4 SEP 2011
  4. Manuscript Received: 14 JUN 2011

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