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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.

Autor: Tan JAMA; Department of Biomedical Science, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia., Kho SL; Department of Biomedical Science, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia., Ngim CF; Department of Paediatrics, School of Medicine and Health Sciences, Monash University Sunway Campus, Selangor, Malaysia., Chua KH; Department of Biomedical Science, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia., Goh AS; Department of Paediatrics, Hospital Pulau Pinang, Jalan Residensi, Penang, Malaysia., Yeoh SL; Department of Paediatrics, Hospital Pulau Pinang, Jalan Residensi, Penang, Malaysia., George E; Assunta Hospital, Petaling Jaya, Selangor, Malaysia.

Publikováno v: Scientific reports [Sci Rep] 2016 Jun 08; Vol. 6, pp. 26994. Date of Electronic Publication: 2016 Jun 08.

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.

Autor: Tan JA; Department of Biomedical Science, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia., Chin SS, Ong GB, Mohamed Unni MN, Soosay AE, Gudum HR, Kho SL, Chua KH, Chen JJ, George E

Publikováno v: Public health genomics [Public Health Genomics] 2015; Vol. 18 (1), pp. 60-4. Date of Electronic Publication: 2014 Nov 19.

Specific and straightforward molecular investigation of β-thalassemia mutations in the Malaysian Malays and Chinese using direct TaqMan genotyping assays.

Autor: Kho SL; Department of Biomedical Science, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia., Chua KH, George E, Tan JA

Publikováno v: Genetics and molecular research : GMR [Genet Mol Res] 2013 Jul 15; Vol. 12 (3), pp. 2409-15. Date of Electronic Publication: 2013 Jul 15.