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.
A patient with a mild holoprosencephaly spectrum phenotype and heterotaxy and a 1.3 Mb deletion encompassing GLI2†
Article first published online: 21 NOV 2011
Copyright © 2011 Wiley Periodicals, Inc.
American Journal of Medical Genetics Part A
Volume 158A, Issue 1, pages 166–173, January 2012
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
- Issue published online: 19 DEC 2011
- Article first published online: 21 NOV 2011
- Manuscript Accepted: 4 SEP 2011
- Manuscript Received: 14 JUN 2011
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