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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2004 1
2012 5
2013 3
2014 8
2015 3
2016 4
2017 4
2018 3
2019 1
2020 6
2021 4
2022 3
2023 3
2024 0

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41 results

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Page 1
Syndromes with supernumerary teeth.
Lubinsky M, Kantaputra PN. Lubinsky M, et al. Among authors: kantaputra pn. Am J Med Genet A. 2016 Oct;170(10):2611-6. doi: 10.1002/ajmg.a.37763. Epub 2016 Jun 2. Am J Med Genet A. 2016. PMID: 27250821 Review.
Making extra teeth: Lessons from a TRPS1 mutation.
Kunotai W, Ananpornruedee P, Lubinsky M, Pruksametanan A, Kantaputra PN. Kunotai W, et al. Among authors: kantaputra pn. Am J Med Genet A. 2017 Jan;173(1):99-107. doi: 10.1002/ajmg.a.37967. Epub 2016 Oct 5. Am J Med Genet A. 2017. PMID: 27706911 Review.
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. 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
TFAP2B mutation and dental anomalies.
Tanasubsinn N, Sittiwangkul R, Pongprot Y, Kawasaki K, Ohazama A, Sastraruji T, Kaewgahya M, Kantaputra PN. Tanasubsinn N, et al. Among authors: kantaputra pn. J Hum Genet. 2017 Aug;62(8):769-775. doi: 10.1038/jhg.2017.37. Epub 2017 Apr 6. J Hum Genet. 2017. PMID: 28381879 Free PMC article.
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.
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.
Enamel-renal-gingival syndrome and FAM20A mutations.
Kantaputra PN, Kaewgahya M, Khemaleelakul U, Dejkhamron P, Sutthimethakorn S, Thongboonkerd V, Iamaroon A. Kantaputra PN, et al. Am J Med Genet A. 2014 Jan;164A(1):1-9. doi: 10.1002/ajmg.a.36187. Epub 2013 Nov 20. Am J Med Genet A. 2014. PMID: 24259279
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
41 results