Balkan Journal of Medical Genetics

THE IMPORTANCE OF MOLECULAR BIOLOGICAL ANALYSIS FOR THE LABORATORY DIAGNOSTIC OF HOMOZYGOUS HAEMOGLOBIN MALAY
Bahar R, Zulkafli Z, Zulkeflee RH, Hassan MN, Rahman Wan S Wan Ab, Noor NH M, Ramli M, Hussin A, Abdullah AD, Iberahim S, Abdullah M, Yusoff S M
*Corresponding Author: Dr Zefarina Zulkafli, School of Medical Sciences, Universiti Sains Malaysia, 16150, Kubang Kerian, Kelantan. Email address: zefarinazulkafli@gmail.com
page: 65

REFERENCES

1. Thein SL. The molecular basis of β-thalassemia. Cold Spring Harb Perspect Med. 2013;3(5):1–24. 2. Traivaree C, Boonyawat B, Monsareenusorn C. Mo- lecular analysis of beta-globin gene mutations among Thai beta-thalassemia children: results from a single center study. Appl Clin Genet. 2014;253. 3. Lee YK, Kim HJ, Lee K, Park SH, Song SH, Seong MW, et al. Recent progress in laboratory diagnosis of thalassemia and hemoglobinopathy: A study by the Korean Red Blood Cell Disorder Working Party of the Korean Society of Hematology. Blood Res. 2019;54(1):17–22. 4. Brancaleoni V, Di Pierro E, Motta I, Cappellini MD. Laboratory diagnosis of thalassemia. Int J Lab He- matol [Internet]. 2016 May 1 [cited 2022 Feb 20];38 Suppl 1:32–40. Available from: https://pubmed.ncbi. nlm.nih.gov/27183541/ 5. Amran HS, Sarijan N, Sathar J, Md Noor S. Case series of homozygous and compound heterozygo- sity of Hb Malay, the diagnostic features and trans- fusion requirements. J Biomed Clin Sci [Internet]. 2017;3(2):10–7. Available from: http://apps.amdi. usm.my/journal/index.php/jbcs/article/view/180 6. George E, Huisman THJ, Yang KG, Kutlari F, Wilson JB, Kutlar A, et al. First observation of haemoglobin Malay. Med J Malaysia. 1989;44(3):259–62. 7. Yusoff YM, Hamid FS, Esa E, Aziz NA, Hassan S, Anoar SZ, et al. Molecular and Haematological Char- acterisation of Hb Malay in Malaysian Population. Asian J Med Biomed [Internet]. 2018 [cited 2022 Feb 20]; Available from: https://www.semanticscholar. org/paper/Molecular-and-Haematological-Charac- terisation-of-Hb-Yusoff-Hamid/5fd503a15bf5e5a0 39200a868e47b1a2c8b09fdf 8. Yamsri S, Singha K, Prajantasen T, Taweenan W, Fucharoen G, Sanchaisuriya K, Fucharoen S. A large cohort of β(+)-thalassemia in Thailand: molecular, hematological and diagnostic considerations. Blood Cells Mol Dis. 2015 Feb;54(2):164-9. doi: 9. Sharma S, Sehgal S, Das R, Gulati S. Phenotypic heterogeneity of delta-beta thalassemia. Indian J Pathol Microbiol [Internet]. 2019 Jan 1 [cited 2022 Feb 20];62(1):185–6. Available from: https://pubmed. ncbi.nlm.nih.gov/30706898/ 10. Karim MUA, Moinuddin, Babar SU. Cap +1 mu- tation; an unsuspected cause of beta thalassae- mia transmission in Pakistan. Turkish J Hematol. 2009;26(4):167–70.

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