Kantaputra PN - Search Results

1

Heterozygous mutation in the SAM domain of p63 underlies Rapp-Hodgkin ectodermal dysplasia.

Kantaputra PN, Hamada T, Kumchai T, McGrath JA. Kantaputra PN, et al. J Dent Res. 2003 Jun;82(6):433-7. doi: 10.1177/154405910308200606. J Dent Res. 2003. PMID: 12766194

2

Rapp-Hodgkin syndrome with palmoplantar keratoderma, glossy tongue, congenital absence of lingual frenum and of sublingual caruncles: newly recognized findings.

Kantaputra PN, Pruksachatkunakorn C, Vanittanakom P. Kantaputra PN, et al. Am J Med Genet. 1998 Oct 12;79(5):343-6. Am J Med Genet. 1998. PMID: 9779799

3

Tricho-rhino-phalangeal syndrome with supernumerary teeth.

Kantaputra P, Miletich I, Lüdecke HJ, Suzuki EY, Praphanphoj V, Shivdasani R, Wuelling M, Vortkamp A, Napierala D, Sharpe PT. Kantaputra P, et al. J Dent Res. 2008 Nov;87(11):1027-31. doi: 10.1177/154405910808701102. J Dent Res. 2008. PMID: 18946009

4

Expanding the phenotypic spectrum of acro-cardio-facial syndrome (ACFS): Exclusion of P63 mutation.

Tanpaiboon P, Sittiwangkul R, Dejkhamron P, Srikummool M, Sripathomsawat W, Kantaputra P. Tanpaiboon P, et al. Am J Med Genet A. 2009 Aug;149A(8):1749-53. doi: 10.1002/ajmg.a.32737. Am J Med Genet A. 2009. PMID: 19606477

5

Cleft lip with cleft palate, ankyloglossia, and hypodontia are associated with TBX22 mutations.

Kantaputra PN, Paramee M, Kaewkhampa A, Hoshino A, Lees M, McEntagart M, Masrour N, Moore GE, Pauws E, Stanier P. Kantaputra PN, et al. J Dent Res. 2011 Apr;90(4):450-5. doi: 10.1177/0022034510391052. Epub 2011 Jan 19. J Dent Res. 2011. PMID: 21248356 Free article.

6

Mutation in SAM domain of TP63 is associated with nonsyndromic cleft lip and palate and cleft palate.

Kantaputra PN, Malaivijitnond S, Vieira AR, Heering J, Dötsch V, Khankasikum T, Sripathomsawat W. Kantaputra PN, et al. Am J Med Genet A. 2011 Jun;155A(6):1432-6. doi: 10.1002/ajmg.a.34011. Epub 2011 May 12. Am J Med Genet A. 2011. PMID: 21567929

7

Split hand-split foot-ectodermal dysplasia and amelogenesis imperfecta with a TP63 mutation.

Kantaputra PN, Matangkasombut O, Sripathomsawat W. Kantaputra PN, et al. Am J Med Genet A. 2012 Jan;158A(1):188-92. doi: 10.1002/ajmg.a.34356. Epub 2011 Nov 7. Am J Med Genet A. 2012. PMID: 22065540

8

GREMLIN 2 Mutations and Dental Anomalies.

Kantaputra PN, Kaewgahya M, Hatsadaloi A, Vogel P, Kawasaki K, Ohazama A, Ketudat Cairns JR. Kantaputra PN, et al. J Dent Res. 2015 Dec;94(12):1646-52. doi: 10.1177/0022034515608168. Epub 2015 Sep 28. J Dent Res. 2015. PMID: 26416033

9

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. 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.

10

WNT10A, dermatology and dentistry.

Doolan BJ, Onoufriadis A, Kantaputra P, McGrath JA. Doolan BJ, et al. Br J Dermatol. 2021 Dec;185(6):1105-1111. doi: 10.1111/bjd.20601. Epub 2021 Sep 7. Br J Dermatol. 2021. PMID: 34184264 Review.

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