SETBP1 mutations in two Thai patients with Schinzel–Giedion syndrome
Version of Record online: 4 MAR 2011
© 2011 John Wiley & Sons A/S
Volume 79, Issue 4, pages 391–393, April 2011
How to Cite
Suphapeetiporn, K., Srichomthong, C. and Shotelersuk, V. (2011), SETBP1 mutations in two Thai patients with Schinzel–Giedion syndrome. Clinical Genetics, 79: 391–393. doi: 10.1111/j.1399-0004.2010.01552.x
- Issue online: 4 MAR 2011
- Version of Record online: 4 MAR 2011
The following Supporting information is available for this article:
Fig. S1. Lateral view of a skull X-ray of Case 1 demonstrating the wide occipital synchondrosis.
Fig. S2. Lateral view of a skull X-ray of Case 2 demonstrating the wide occipital synchondrosis.
Additional Supporting information may be found in the online version of this article.
|CGE_1552_sm_fig1.jpg||168K||Supporting info item|
|CGE_1552_sm_fig2.jpg||164K||Supporting info item|
Please note: Wiley Blackwell is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.