These authors contributed equally to this work.
A disease causing deletion of 29 base pairs in intron 15 in the MKS1 gene is highly associated with the campomelic variant of the Meckel–Gruber syndrome
Article first published online: 5 SEP 2007
2007 Blackwell Munksgaard
Volume 72, Issue 5, pages 454–459, November 2007
How to Cite
Auber, B., Burfeind, P., Herold, S., Schoner, K., Simson, G., Rauskolb, R. and Rehder, H. (2007), A disease causing deletion of 29 base pairs in intron 15 in the MKS1 gene is highly associated with the campomelic variant of the Meckel–Gruber syndrome. Clinical Genetics, 72: 454–459. doi: 10.1111/j.1399-0004.2007.00880.x
- Issue published online: 10 SEP 2007
- Article first published online: 5 SEP 2007
- Received 13 March 2007, revised and accepted for publication 27 June 2007
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