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Prevalence of 3.7 and 4.2 deletions in Sudanese patients with red cells hypochromia and microcytosis.
- Published in:
- BMC Research Notes, 2020, v. 13, n. 1, p. 1, doi. 10.1186/s13104-020-4933-5
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- Article
Molecular Characterization of α:- and β-Thalassaemia among Malay Patients.
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- International Journal of Molecular Sciences, 2014, v. 15, n. 5, p. 8835, doi. 10.3390/ijms15058835
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- Article
Distribution of Alpha Thalassaemia Gene Variants in Diverse Ethnic Populations in Malaysia: Data from the Institute for Medical Research.
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- International Journal of Molecular Sciences, 2013, v. 14, n. 9, p. 18599, doi. 10.3390/ijms140918599
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- Article
First Two Cases of Fungal Infections Associated with Multi-drug Resistant Yeast, Fereydounia khargensis.
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- Mycopathologia, 2016, v. 181, n. 7/8, p. 531, doi. 10.1007/s11046-016-0002-y
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- Article
A Conceptual Study on Green Management Practices in Banking Industry.
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- Global Business & Management Research, 2022, v. 14, p. 298
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- Article
β-globin Gene Mutations Among β-thalassemia and β-variant patients in a teaching Hospital in Universiti Sains Malaysia, Kubang Kerian, Kelantan.
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- Gazi Medical Journal, 2022, v. 33, n. 3, p. 215, doi. 10.12996/gmj.2022.51
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- Article
A nonsense mutation in exon 8 of the APC gene (Arg283Ter) causes clinically variable FAP in a Malaysian Chinese family.
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- Cancer Science, 2003, v. 94, n. 8, p. 725, doi. 10.1111/j.1349-7006.2003.tb01509.x
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- Article
Detection of β -globin Gene Mutations Among β -thalassaemia Carriers and Patients in Malaysia: Application of Multiplex Amplification Refractory Mutation System-Polymerase Chain Reaction.
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- Malaysian Journal of Medical Sciences, 2013, v. 20, n. 1, p. 13
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- Article
A novel single gene deletion (-α<sup>MAL3.5</sup>) giving rise to silent α thalassemia carrier removing the entire HBA2 gene observed in two Chinese patients with Hb H disease: case report of two probands.
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- Thalassemia Reports, 2015, v. 5, n. 1, p. 12, doi. 10.4081/thal.2015.4675
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- Article
Molecular Characterisation of α- and β-Thalassaemia among Indigenous Senoi Orang Asli Communities in Peninsular Malaysia.
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- Annals of Human Genetics, 2017, v. 81, n. 5, p. 205, doi. 10.1111/ahg.12201
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- Article
Rare cause of transfusion‐dependent hemolytic anemia: A case report of HbE/Hb Nottingham and literature review.
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- Pediatric Blood & Cancer, 2022, v. 69, n. 9, p. 1, doi. 10.1002/pbc.29629
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- Article
Haemoglobin Sickle D Punjab: - A Case Report.
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- Medical Journal of Malaysia, 2014, v. 69, n. 1, p. 42
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- Article
Distribution of alpha thalassaemia in 16 year old Malaysian Students in Penang, Melaka and Sabah.
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- Medical Journal of Malaysia, 2012, v. 67, n. 6, p. 565
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- Article