Intachai W - Search Results

1

Clouston syndrome with dental anomalies, micropores of hair shafts and absence of palmoplantar keratoderma.

Kantaputra PN, Intachai W, Carlson BM, Pruksachatkunakorn C. Kantaputra PN, et al. Among authors: intachai w. J Dermatol. 2020 Mar;47(3):e90-e91. doi: 10.1111/1346-8138.15236. Epub 2020 Jan 21. J Dermatol. 2020. PMID: 31960478 Free article. No abstract available.

2

All enamel is not created equal:Supports from a novel FAM83H mutation.

Kantaputra PN, Intachai W, Auychai P. Kantaputra PN, et al. Among authors: intachai w. Am J Med Genet A. 2016 Jan;170A(1):273-6. doi: 10.1002/ajmg.a.37406. Epub 2015 Oct 20. Am J Med Genet A. 2016. PMID: 26481691 No abstract available.

3

WNT10B mutations associated with isolated dental anomalies.

Kantaputra PN, Hutsadaloi A, Kaewgahya M, Intachai W, German R, Koparal M, Leethanakul C, Tolun A, Ketudat Cairns JR. Kantaputra PN, et al. Among authors: intachai w. Clin Genet. 2018 May;93(5):992-999. doi: 10.1111/cge.13218. Epub 2018 Mar 2. Clin Genet. 2018. PMID: 29364501

4

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: intachai w. 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

5

Osteogenesis imperfecta with ectopic mineralizations in dentin and cementum and a COL1A2 mutation.

Kantaputra PN, Sirirungruangsarn Y, Intachai W, Ngamphiw C, Tongsima S, Dejkhamron P. Kantaputra PN, et al. Among authors: intachai w. J Hum Genet. 2018 Jul;63(7):811-820. doi: 10.1038/s10038-018-0448-5. Epub 2018 Apr 10. J Hum Genet. 2018. PMID: 29636545

6

Isolated dentinogenesis imperfecta with glass-like enamel caused by COL1A2 mutation.

Kantaputra PN, Chinadet W, Intachai W, Ngamphiw C, Ketudat Cairns JR, Tongsima S. Kantaputra PN, et al. Among authors: intachai w. Am J Med Genet A. 2018 Dec;176(12):2919-2923. doi: 10.1002/ajmg.a.40501. Epub 2018 Aug 27. Am J Med Genet A. 2018. PMID: 30152103 No abstract available.

7

WNT1-associated osteogenesis imperfecta with atrophic frontal lobes and arachnoid cysts.

Kantaputra PN, Sirirungruangsarn Y, Visrutaratna P, Petcharunpaisan S, Carlson BM, Intachai W, Sudasna J, Kampuansai J, Dejkhamron P. Kantaputra PN, et al. Among authors: intachai w. J Hum Genet. 2019 Apr;64(4):291-296. doi: 10.1038/s10038-019-0565-9. Epub 2019 Jan 28. J Hum Genet. 2019. PMID: 30692598

8

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

9

Clouston syndrome with pili canaliculi, pili torti, overgrown hyponychium, onycholysis, taurodontism and absence of palmoplantar keratoderma.

Kantaputra P, Intachai W, Kawasaki K, Ohazama A, Carlson B, Quarto N, Pruksachatkun C, Chuamanochan M. Kantaputra P, et al. Among authors: intachai w. J Dermatol. 2020 Jun;47(6):e230-e232. doi: 10.1111/1346-8138.15333. Epub 2020 Mar 27. J Dermatol. 2020. PMID: 32220018 Free article. No abstract available.

10

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

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