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SERPINA1, generalized pustular psoriasis, and adult-onset immunodeficiency.
Kantaputra P, Chaowattanapanit S, Kiratikanon S, Chaiwarith R, Choonhakarn C, Intachai W, Quarto N, Tongsima S, Ketudat Cairns JR, Ngamphiw C, McGrath JA, Chuamanochan M. Kantaputra P, et al. Among authors: ketudat cairns jr. J Dermatol. 2021 Oct;48(10):1597-1601. doi: 10.1111/1346-8138.16081. Epub 2021 Aug 12. J Dermatol. 2021. PMID: 34390020
Periodontal disease and FAM20A mutations.
Kantaputra PN, Bongkochwilawan C, Lubinsky M, Pata S, Kaewgahya M, Tong HJ, Ketudat Cairns JR, Guven Y, Chaisrisookumporn N. Kantaputra PN, et al. Among authors: ketudat cairns jr. J Hum Genet. 2017 Jul;62(7):679-686. doi: 10.1038/jhg.2017.26. Epub 2017 Mar 16. J Hum Genet. 2017. PMID: 28298625
Split hand-foot malformation and a novel WNT10B mutation.
Kantaputra PN, Kapoor S, Verma P, Intachai W, Ketudat Cairns JR. Kantaputra PN, et al. Among authors: ketudat cairns jr. Eur J Med Genet. 2018 Jul;61(7):372-375. doi: 10.1016/j.ejmg.2018.02.001. Epub 2018 Feb 7. Eur J Med Genet. 2018. PMID: 29427788
Oral manifestations in patients and dogs with mucopolysaccharidosis Type VII.
Kantaputra PN, Smith LJ, Casal ML, Kuptanon C, Chang YC, Nampoothiri S, Paiyarom A, Veerasakulwong T, Trachoo O, Ketudat Cairns JR, Chinadet W, Tanpaiboon P. Kantaputra PN, et al. Among authors: ketudat cairns jr. Am J Med Genet A. 2019 Mar;179(3):486-493. doi: 10.1002/ajmg.a.61034. Epub 2019 Jan 17. Am J Med Genet A. 2019. PMID: 30653816 Free PMC article.
ADAMTSL1 and mandibular prognathism.
Kantaputra PN, Pruksametanan A, Phondee N, Hutsadaloi A, Intachai W, Kawasaki K, Ohazama A, Ngamphiw C, Tongsima S, Ketudat Cairns JR, Tripuwabhrut P. Kantaputra PN, et al. Among authors: ketudat cairns jr. Clin Genet. 2019 Apr;95(4):507-515. doi: 10.1111/cge.13519. Clin Genet. 2019. PMID: 30714143
Are dental anomalies associated with Tietz syndrome?
Kantaputra PN, Intachai W, Carlson B, Olsen B, Ngaohirunphat S, Sri-Oon J, Ketudat Cairns JR, Choovuthayakorn J. Kantaputra PN, et al. Among authors: ketudat cairns jr. Eur J Dermatol. 2020 Dec 1;30(6):734-736. doi: 10.1684/ejd.2020.3905. Eur J Dermatol. 2020. PMID: 33459262 No abstract available.
A novel P3H1 mutation is associated with osteogenesis imperfecta type VIII and dental anomalies.
Kantaputra PN, Dejkhamron P, Intachai W, Ngamphiw C, Ketudat Cairns JR, Kawasaki K, Ohazama A, Olsen B, Tongsima S, Angkurawaranon S. Kantaputra PN, et al. Among authors: ketudat cairns jr. Oral Surg Oral Med Oral Pathol Oral Radiol. 2021 Dec;132(6):e198-e207. doi: 10.1016/j.oooo.2021.01.023. Epub 2021 Jan 28. Oral Surg Oral Med Oral Pathol Oral Radiol. 2021. PMID: 33737016
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