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Repeat expansion and methylation-sensitive triplet-primed polymerase chain reaction for fragile X mental retardation 1 gene screening in institutionalised intellectually disabled individuals.
Sihombing NRB, Cai S, Wong DPW, Guan M, Chong SS, Faradz SMH, Winarni TI. Sihombing NRB, et al. Among authors: winarni ti. Singapore Med J. 2021 Mar;62(3):143-148. doi: 10.11622/smedj.2020009. Epub 2020 Jan 28. Singapore Med J. 2021. PMID: 31989181 Free PMC article.
A cytogenetic study in a large population of intellectually disabled Indonesians.
Mundhofir FE, Winarni TI, van Bon BW, Aminah S, Nillesen WM, Merkx G, Smeets D, Hamel BC, Faradz SM, Yntema HG. Mundhofir FE, et al. Among authors: winarni ti. Genet Test Mol Biomarkers. 2012 May;16(5):412-7. doi: 10.1089/gtmb.2011.0157. Epub 2011 Dec 22. Genet Test Mol Biomarkers. 2012. PMID: 22191675 Free article.
The fragile X-associated tremor ataxia syndrome (FXTAS) in Indonesia.
Winarni TI, Mundhofir FE, Ediati A, Belladona M, Nillesen WM, Yntema HG, Hamel BC, Faradz SM, Hagerman RJ. Winarni TI, et al. Clin Genet. 2013 Mar;83(3):263-8. doi: 10.1111/j.1399-0004.2012.01899.x. Epub 2012 Jun 6. Clin Genet. 2013. PMID: 22568721
Surveillance and prevalence of fragile X syndrome in Indonesia.
Sihombing NRB, Winarni TI, Utari A, van Bokhoven H, Hagerman RJ, Faradz SM. Sihombing NRB, et al. Among authors: winarni ti. Intractable Rare Dis Res. 2021 Feb;10(1):11-16. doi: 10.5582/irdr.2020.03101. Intractable Rare Dis Res. 2021. PMID: 33614370 Free PMC article. Review.
37 results