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