Keong TM - Search Results

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Analysis of complications following multidisciplinary functional intervention in paediatric craniomaxillofacial deformities.

Hariri F, Abdullah MF, Adam KBC, Bahuri NFA, Kulasegarah J, Nathan AM, Ismail F, Khaliddin N, May CM, Chan L, Keong TM, Ganesan D, Rahman ZAA. Hariri F, et al. Among authors: keong tm. Int J Oral Maxillofac Surg. 2021 Apr;50(4):457-462. doi: 10.1016/j.ijom.2020.08.002. Epub 2020 Sep 3. Int J Oral Maxillofac Surg. 2021. PMID: 32891466

Chromosomal 16p microdeletion in Rubinstein-Taybi syndrome detected by oligonucleotide-based array comparative genomic hybridization: a case report.

Mohd Fadley MA, Ismail A, Keong TM, Yusoff NM, Zakaria Z. Mohd Fadley MA, et al. Among authors: keong tm. J Med Case Rep. 2012 Jan 23;6:30. doi: 10.1186/1752-1947-6-30. J Med Case Rep. 2012. PMID: 22269667 Free PMC article.

Harmonizing the interpretation of genetic variants across the world: the Malaysian experience.

Hassan NN, Plazzer JP, Smith TD, Halim-Fikri H, Macrae F, Zubaidi AA, Zilfalil BA; Members of Malaysian Node of HVP. Hassan NN, et al. BMC Res Notes. 2016 Feb 26;9:125. doi: 10.1186/s13104-015-1798-0. BMC Res Notes. 2016. PMID: 26915360 Free PMC article.

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