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Year | Number of Results |
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2013 | 1 |
2014 | 1 |
2015 | 3 |
2016 | 1 |
2024 | 0 |
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DNA studies are necessary for accurate patient diagnosis in compound heterozygosity for Hb Adana (HBA2:c.179>A) with deletional or nondeletional α-thalassaemia.
Sci Rep. 2016 Jun 8;6:26994. doi: 10.1038/srep26994.
Sci Rep. 2016.
PMID: 27271331
Free PMC article.
Non-Invasive DNA Sampling for Molecular Analysis of Beta-Thalassemia: Amiable Alternative Sampling Methods with Accurate Results for Pediatric Patients.
Abd Rahim MR, Kho SL, Kuppusamy UR, Tan JA.
Abd Rahim MR, et al. Among authors: kho sl.
Clin Lab. 2015;61(9):1325-30. doi: 10.7754/clin.lab.2015.150218.
Clin Lab. 2015.
PMID: 26554253
Item in Clipboard
A novel gap-PCR with high resolution melting analysis for the detection of α-thalassaemia Southeast Asian and Filipino β°-thalassaemia deletion.
Kho SL, Chua KH, George E, Tan JA.
Kho SL, et al.
Sci Rep. 2015 Sep 14;5:13937. doi: 10.1038/srep13937.
Sci Rep. 2015.
PMID: 26365497
Free PMC article.
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Transfusion-dependent thalassemia in Northern Sarawak: a molecular study to identify different genotypes in the multi-ethnic groups and the importance of genomic sequencing in unstudied populations.
Tan JA, Chin SS, Ong GB, Mohamed Unni MN, Soosay AE, Gudum HR, Kho SL, Chua KH, Chen JJ, George E.
Tan JA, et al. Among authors: kho sl.
Public Health Genomics. 2015;18(1):60-4. doi: 10.1159/000368342. Epub 2014 Nov 19.
Public Health Genomics. 2015.
PMID: 25412720
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High throughput molecular confirmation of β-thalassemia mutations using novel TaqMan probes.
Kho SL, Chua KH, George E, Tan JA.
Kho SL, et al.
Sensors (Basel). 2013 Feb 18;13(2):2506-14. doi: 10.3390/s130202506.
Sensors (Basel). 2013.
PMID: 23429513
Free PMC article.
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