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Page 1
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: intachai w. Clin Genet. 2019 Apr;95(4):507-515. doi: 10.1111/cge.13519. Clin Genet. 2019. PMID: 30714143
SERPINB3, Adult-Onset Immunodeficiency, and Generalized Pustular Psoriasis.
Kantaputra P, Daroontum T, Chuamanochan M, Chaowattanapanit S, Kiratikanon S, Choonhakarn C, Intachai W, Olsen B, Tongsima S, Ngamphiw C, Pontisso P, Cox TC, Ounjai P. Kantaputra P, et al. Among authors: intachai w. Genes (Basel). 2023 Jan 19;14(2):266. doi: 10.3390/genes14020266. Genes (Basel). 2023. PMID: 36833193 Free PMC article.
LRP4 mutations, dental anomalies, and oral exostoses.
Kantaputra P, Panichkul W, Sillapasorn P, Adisornkanj P, Kitsadayurach P, Kaewgaya M, Intachai W, Olsen B, Ngamphiw C, Leethanakul C, Jatooratthawichot P, Ketudat Cairns JR, Tongsima S. Kantaputra P, et al. Among authors: intachai w. Int J Paediatr Dent. 2023 Nov 27. doi: 10.1111/ipd.13141. Online ahead of print. Int J Paediatr Dent. 2023. PMID: 38013205
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: intachai w. J Dermatol. 2021 Oct;48(10):1597-1601. doi: 10.1111/1346-8138.16081. Epub 2021 Aug 12. J Dermatol. 2021. PMID: 34390020
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: intachai w. 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.
Novel Dental Anomaly-associated Mutations in WNT10A Protein Binding Sites.
Kantaputra P, Jatooratthawichot P, Tantachamroon O, Nanekrungsan K, Intachai W, Olsen B, Tongsima S, Ngamphiw C, Cairns JRK. Kantaputra P, et al. Among authors: intachai w. Int Dent J. 2023 Feb;73(1):79-86. doi: 10.1016/j.identj.2022.04.006. Epub 2022 May 7. Int Dent J. 2023. PMID: 35537890 Free PMC article.
A truncating variant in SERPINA3, skin pustules and adult-onset immunodeficiency.
Kantaputra PN, Chuamanochan M, Kiratikanon S, Chiewchanvit S, Chaiwarith R, Intachai W, Quarto N, Tongsima S, McGrath JA, Ngamphiw C. Kantaputra PN, et al. Among authors: intachai w. J Dermatol. 2021 Aug;48(8):e370-e371. doi: 10.1111/1346-8138.15942. Epub 2021 May 7. J Dermatol. 2021. PMID: 33961311 No abstract available.
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. Among authors: intachai w. Eur J Orthod. 2021 Jan 29;43(1):45-50. doi: 10.1093/ejo/cjaa023. Eur J Orthod. 2021. PMID: 32255174
Clinical and Genetic Studies of the First Monozygotic Twins with Pfeiffer Syndrome.
Kantaputra PN, Angkurawaranon S, Khwanngern K, Ngamphiw C, Intachai W, Adisornkanj P, Tongsima S, Olsen B, Sonsuwan N, Katanyuwong K. Kantaputra PN, et al. Among authors: intachai w. Genes (Basel). 2022 Oct 13;13(10):1850. doi: 10.3390/genes13101850. Genes (Basel). 2022. PMID: 36292735 Free PMC article.
34 results