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Pathogenic mechanism of mutations in the thyroid hormone receptor β gene.
Pongjantarasatian S, Wacharasindhu S, Tongkobpetch S, Suphapeetiporn K, Shotelersuk V. Pongjantarasatian S, et al. Among authors: tongkobpetch s. J Endocrinol Invest. 2012 Jun;35(6):557-61. doi: 10.3275/7876. Epub 2011 Jul 27. J Endocrinol Invest. 2012. PMID: 21795843
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