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WNT10A variant and severe scoliosis?
Kantaputra P, Olsen B, McGrath JA. Kantaputra P, et al. J Dermatol. 2022 May;49(5):e183-e184. doi: 10.1111/1346-8138.16313. Epub 2022 Feb 21. J Dermatol. 2022. PMID: 35191062 No abstract available.
WNT10A and isolated hypodontia.
Kantaputra P, Sripathomsawat W. Kantaputra P, et al. Am J Med Genet A. 2011 May;155A(5):1119-22. doi: 10.1002/ajmg.a.33840. Epub 2011 Apr 11. Am J Med Genet A. 2011. PMID: 21484994
Tricho-odonto-onycho-dermal dysplasia and WNT10A mutations.
Kantaputra P, Kaewgahya M, Jotikasthira D, Kantaputra W. Kantaputra P, et al. Among authors: kantaputra w. Am J Med Genet A. 2014 Apr;164A(4):1041-8. doi: 10.1002/ajmg.a.36388. Epub 2014 Jan 23. Am J Med Genet A. 2014. PMID: 24458874
Juberg-Hayward syndrome is a cohesinopathy, caused by mutation in ESCO2.
Kantaputra PN, Dejkhamron P, Intachai W, Ngamphiw C, Kawasaki K, Ohazama A, Krisanaprakornkit S, Olsen B, Tongsima S, Ketudat Cairns JR. Kantaputra PN, et al. Eur J Orthod. 2021 Jan 29;43(1):45-50. doi: 10.1093/ejo/cjaa023. Eur J Orthod. 2021. PMID: 32255174
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. 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.
116 results