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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2019 | 2 |
2020 | 1 |
2021 | 2 |
2022 | 1 |
2024 | 0 |
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Page 1
Age-related dental phenotypes and tooth characteristics of FAM83H-associated hypocalcified amelogenesis imperfecta.
Oral Dis. 2022 Apr;28(3):734-744. doi: 10.1111/odi.13780. Epub 2021 Feb 4.
Oral Dis. 2022.
PMID: 33486840
The Thai reference exome (T-REx) variant database.
Shotelersuk V, Wichadakul D, Ngamphiw C, Srichomthong C, Phokaew C, Wilantho A, Pakchuen S, Nakhonsri V, Shaw PJ, Wasitthankasem R, Piriyapongsa J, Wangkumhang P, Assawapitaksakul A, Chetruengchai W, Lapphra K, Khuninthong A, Makarawate P, Suphapeetiporn K, Mahasirimongkol S, Satproedprai N, Porntaveetus T, Pisitkun P, Praphanphoj V, Kantaputra P, Tassaneeyakul W, Tongsima S.
Shotelersuk V, et al.
Clin Genet. 2021 Dec;100(6):703-712. doi: 10.1111/cge.14060. Epub 2021 Sep 22.
Clin Genet. 2021.
PMID: 34496037
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Genotype-phenotype correlation and expansion of orodental anomalies in LTBP3-related disorders.
Intarak N, Theerapanon T, Thaweesapphithak S, Suphapeetiporn K, Porntaveetus T, Shotelersuk V.
Intarak N, et al.
Mol Genet Genomics. 2019 Jun;294(3):773-787. doi: 10.1007/s00438-019-01547-x. Epub 2019 Mar 18.
Mol Genet Genomics. 2019.
PMID: 30887145
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Female-restricted syndromic intellectual disability in a patient from Thailand.
Sinthuwiwat T, Ittiwut C, Porntaveetus T, Shotelersuk V.
Sinthuwiwat T, et al.
Am J Med Genet A. 2019 May;179(5):758-761. doi: 10.1002/ajmg.a.61106. Epub 2019 Mar 3.
Am J Med Genet A. 2019.
PMID: 30828969
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Four novel mutations of FAM20A in amelogenesis imperfecta type IG and review of literature for its genotype and phenotype spectra.
Nitayavardhana I, Theerapanon T, Srichomthong C, Piwluang S, Wichadakul D, Porntaveetus T, Shotelersuk V.
Nitayavardhana I, et al.
Mol Genet Genomics. 2020 Jul;295(4):923-931. doi: 10.1007/s00438-020-01668-8. Epub 2020 Apr 3.
Mol Genet Genomics. 2020.
PMID: 32246227
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