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FOXE1 mutations in Thai patients with oral clefts.
Srichomthong C, Ittiwut R, Siriwan P, Suphapeetiporn K, Shotelersuk V. Srichomthong C, et al. Among authors: ittiwut r. Genet Res (Camb). 2013 Oct;95(5):133-7. doi: 10.1017/S0016672313000177. Epub 2013 Nov 20. Genet Res (Camb). 2013. PMID: 24252547
Novel mutations in Thai patients with glanzmann thrombasthenia.
Ittiwut R, Suchartlikitwong P, Kittikalayawong Y, Ittiwut C, Prasopsanti K, Sosothikul D, Shotelersuk V, Suphapeetiporn K. Ittiwut R, et al. Among authors: ittiwut c. Eur J Haematol. 2017 Dec;99(6):520-524. doi: 10.1111/ejh.12965. Epub 2017 Oct 5. Eur J Haematol. 2017. PMID: 28888044
Mutations in Kinesin family member 6 reveal specific role in ependymal cell ciliogenesis and human neurological development.
Konjikusic MJ, Yeetong P, Boswell CW, Lee C, Roberson EC, Ittiwut R, Suphapeetiporn K, Ciruna B, Gurnett CA, Wallingford JB, Shotelersuk V, Gray RS. Konjikusic MJ, et al. Among authors: ittiwut r. PLoS Genet. 2018 Nov 26;14(11):e1007817. doi: 10.1371/journal.pgen.1007817. eCollection 2018 Nov. PLoS Genet. 2018. PMID: 30475797 Free PMC article.
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