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Correction to 'Genotyping of Malaysian G6PD-deficient neonates by reverse dot blot flow-through hybridisation'.
J Hum Genet. 2020 Jul;65(7):635. doi: 10.1038/s10038-020-0766-2.
J Hum Genet. 2020.
PMID: 32385338
Genotyping of Malaysian G6PD-deficient neonates by reverse dot blot flow-through hybridisation.
Alina MF, Azma RZ, Norunaluwar J, Azlin I, Darnina AJ, Cheah FC, Noor-Farisah AR, Siti-Hawa AA, Danny XRK, Zulkifli NF, Ainoon O.
Alina MF, et al. Among authors: azlin i.
J Hum Genet. 2020 Mar;65(3):263-270. doi: 10.1038/s10038-019-0700-7. Epub 2019 Dec 20.
J Hum Genet. 2020.
PMID: 31863082
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Molecular characteristic of alpha thalassaemia among patients diagnosed in UKM Medical Centre.
Azma RZ, Ainoon O, Hafiza A, Azlin I, Noor Farisah AR, Nor Hidayati S, Noor Hamidah H.
Azma RZ, et al. Among authors: azlin i.
Malays J Pathol. 2014 Apr;36(1):27-32.
Malays J Pathol. 2014.
PMID: 24763232
Free article.
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Prevalence of iron deficiency anaemia and thalassaemia trait among undergraduate medical students.
Azma RZ, Ainoon O, Azlin I, Hamenuddin H, Hadi NA, Tatt WK, Syazana IN, Asmaliza AM, Das S, Hamidah NH.
Azma RZ, et al. Among authors: azlin i.
Clin Ter. 2012 Jul;163(4):287-91.
Clin Ter. 2012.
PMID: 23007811
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Prevalence of uridine glucuronosyl transferase 1A1 (UGT1A1) mutations in Malay neonates with severe jaundice.
Azlin I, Wong FL, Ezham M, Hafiza A, Ainoon O.
Azlin I, et al.
Malays J Pathol. 2011 Dec;33(2):95-100.
Malays J Pathol. 2011.
PMID: 22299209
Free article.
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A family study of HbS in a Malay family by molecular analysis.
Hafiza A, Noor HH, Noor FA, Azlin I, Ainoon O.
Hafiza A, et al. Among authors: azlin i.
Malays J Pathol. 2010 Dec;32(2):137-41.
Malays J Pathol. 2010.
PMID: 21329186
Free article.
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HbA2 levels in normal, beta-thalassaemia and haemoglobin E carriers by capillary electrophoresis.
Hafiza A, Malisa MY, Khirotdin RD, Azlin I, Azma Z, Thong MC, Ali IM, Yeoh ZN, Mohd Ishak L, Mohd Radzi NR, Hussin NH.
Hafiza A, et al. Among authors: azlin i.
Malays J Pathol. 2012 Dec;34(2):161-4.
Malays J Pathol. 2012.
PMID: 23424780
Free article.
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Irreversible visual loss and optic nerve dysfunction associated with central retinal vein occlusion in Waldenstrom Macroglobulinemia.
Fadilah SA, Muhaya M, Azlin I.
Fadilah SA, et al. Among authors: azlin i.
Med J Malaysia. 2007 Oct;62(4):349-51.
Med J Malaysia. 2007.
PMID: 18551947
Free article.
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