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Rapid exome sequencing as the first-tier investigation for diagnosis of acutely and severely ill children and adults in Thailand.
Kamolvisit W, Phowthongkum P, Boonsimma P, Kuptanon C, Rojnueangnit K, Wattanasirichaigoon D, Chanvanichtrakool M, Phuaksaman C, Wiromrat P, Srichomthong C, Ittiwut C, Phokaew C, Ittiwut R, Assawapitaksakul A, Chetruengchai W, Buasong A, Suphapeetiporn K, Shotelersuk V. Kamolvisit W, et al. Among authors: ittiwut c, ittiwut r. Clin Genet. 2021 Jul;100(1):100-105. doi: 10.1111/cge.13963. Epub 2021 Apr 13. Clin Genet. 2021. PMID: 33822359
Clinical and molecular characteristics of Thai patients with achondroplasia.
Shotelersuk V, Ittiwut C, Srivuthana S, Wacharasindhu S, Aroonparkmongkol S, Mutirangura A, Poovorawan Y. Shotelersuk V, et al. Among authors: ittiwut c. Southeast Asian J Trop Med Public Health. 2001 Jun;32(2):429-33. Southeast Asian J Trop Med Public Health. 2001. PMID: 11556601
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: ittiwut c. J Craniofac Surg. 2003 Jan;14(1):101-4; discussion 105-7. doi: 10.1097/00001665-200301000-00019. J Craniofac Surg. 2003. PMID: 12544231
NUDT15 c.415C>T increases risk of 6-mercaptopurine induced myelosuppression during maintenance therapy in children with acute lymphoblastic leukemia.
Chiengthong K, Ittiwut C, Muensri S, Sophonphan J, Sosothikul D, Seksan P, Suppipat K, Suphapeetiporn K, Shotelersuk V. Chiengthong K, et al. Among authors: ittiwut c. Haematologica. 2016 Jan;101(1):e24-6. doi: 10.3324/haematol.2015.134775. Epub 2015 Sep 24. Haematologica. 2016. PMID: 26405151 Free PMC article. No abstract available.
58 results