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Mutation spectrum of dystrophin gene in malaysian patients with Duchenne/Becker muscular dystrophy.
J Neurogenet. 2013 Jun;27(1-2):11-5. doi: 10.3109/01677063.2012.762580. Epub 2013 Feb 26.
J Neurogenet. 2013.
PMID: 23438214
Two novel gross deletions of TSC2 in Malaysian patients with tuberous sclerosis complex and TSC2/PKD1 contiguous deletion syndrome.
Ismail NF, Nik Abdul Malik NM, Mohseni J, Rani AM, Hayati F, Salmi AR, Narazah MY, Zabidi-Hussin ZA, Silawati AR, Keng WT, Ngu LH, Sasongko TH.
Ismail NF, et al. Among authors: salmi ar.
Jpn J Clin Oncol. 2014 May;44(5):506-11. doi: 10.1093/jjco/hyu024. Epub 2014 Mar 30.
Jpn J Clin Oncol. 2014.
PMID: 24683199
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A new method for FMR1 gene methylation screening by multiplex methylation-specific real-time polymerase chain reaction.
Elias MH, Ankathil R, Salmi AR, Sudhikaran W, Limprasert P, Zilfalil BA.
Elias MH, et al. Among authors: salmi ar.
Genet Test Mol Biomarkers. 2011 Jun;15(6):387-93. doi: 10.1089/gtmb.2010.0191. Epub 2011 Feb 17.
Genet Test Mol Biomarkers. 2011.
PMID: 21329465
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Hippocampal MR Volumetric Studies in Paediatric Patients with Epilepsy and Normal Controls.
Win Mar Salmah J, Noorfizura A, Mohd Shafie A, Helmy A, Salmi AR, Naing L.
Win Mar Salmah J, et al. Among authors: salmi ar.
Neuroradiol J. 2011 Aug 31;24(4):503-10. doi: 10.1177/197140091102400404. Epub 2011 Sep 2.
Neuroradiol J. 2011.
PMID: 24059706
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Permissibility of prenatal diagnosis and abortion for fetuses with severe genetic disorder: type 1 spinal muscular atrophy.
Sasongko TH, Salmi AR, Zilfalil BA, Albar MA, Mohd Hussin ZA.
Sasongko TH, et al. Among authors: salmi ar.
Ann Saudi Med. 2010 Nov-Dec;30(6):427-31. doi: 10.4103/0256-4947.72259.
Ann Saudi Med. 2010.
PMID: 21060155
Free PMC article.
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