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PDGFRa mutations in humans with isolated cleft palate.
Rattanasopha S, Tongkobpetch S, Srichomthong C, Siriwan P, Suphapeetiporn K, Shotelersuk V. Rattanasopha S, et al. Among authors: tongkobpetch s. Eur J Hum Genet. 2012 Oct;20(10):1058-62. doi: 10.1038/ejhg.2012.55. Epub 2012 Apr 4. Eur J Hum Genet. 2012. PMID: 22473090 Free PMC article.
FGFR2 mutations among Thai children with Crouzon and Apert syndromes.
Shotelersuk V, Mahatumarat C, Ittiwut C, Rojvachiranonda N, Srivuthana S, Wacharasindhu S, Tongkobpetch S. Shotelersuk V, et al. Among authors: tongkobpetch s. J Craniofac Surg. 2003 Jan;14(1):101-4; discussion 105-7. doi: 10.1097/00001665-200301000-00019. J Craniofac Surg. 2003. PMID: 12544231
Expanding the phenotypic spectrum of Caffey disease.
Suphapeetiporn K, Tongkobpetch S, Mahayosnond A, Shotelersuk V. Suphapeetiporn K, et al. Among authors: tongkobpetch s. Clin Genet. 2007 Mar;71(3):280-4. doi: 10.1111/j.1399-0004.2007.00768.x. Clin Genet. 2007. PMID: 17309652
42 results