Search Results - Azma R.Z.

  • Showing 1 - 11 results of 11
Refine Results
  1. 1
    Correction to ‘Genotyping of Malaysian G6PD-deficient neonates by reverse dot blot flow-through hybridisation’ (Journal of Human Genetics, (2020), 65, 3, (263-270), 10.1038/s10038-019-0700-7)

    Correction to ‘Genotyping of Malaysian G6PD-deficient neonates by reverse dot blot flow-through hybridisation’ (Journal of Human Genetics, (2020), 65, 3, (263-270), 10.1038/s10038-... by Alina M.F., Azma R.Z., Norunaluwar J., Azlin I., Darnina A.J., Cheah F.C., Noor-Farisah A.R., Siti-Hawa A.A., Danny X.R.K., Zulkifli N.F., Ainoon O.

    Published 2024
    journal::journal article
    Save to List
    Saved in:
  2. 2
    Detection of Haemoglobin S using Multiplex Ligation-Dependent Probe Amplification and Flow-through Hybridization Techniques: Experience in a Tertiary Hospital

    Detection of Haemoglobin S using Multiplex Ligation-Dependent Probe Amplification and Flow-through Hybridization Techniques: Experience in a Tertiary Hospital by Wee, S. Y., Hafiza, A., Azma, R. Z., Norunaluwar, J., Azlin, I, Malisa, M. Y., Qistina, W. N., Ainoon, O.

    Published 2024
    Article
    Save to List
    Saved in:
  3. 3
    Sickle Cell Case Series

    Sickle Cell Case Series by Wee S Y, Azma R Z, Hafiza A, Norunaluwar J, Malisa MY, Qistina WN, Ainoon O

    Published 2024
    Article
    Save to List
    Saved in:
  4. 4
    A case series of α-thalassemia intermedia due to compound heterozygosity for Hb Adana [HBA2: C179G>A (or HBA1); P.Gly60Asp] with other α-thalassemias in malay families

    A case series of α-thalassemia intermedia due to compound heterozygosity for Hb Adana [HBA2: C179G>A (or HBA1); P.Gly60Asp] with other α-thalassemias in malay families by Alauddin H., Jaapar N.-A., Azma R.Z., Ithnin A., Razak N.-F.A., Loh C.-K., Alias H., Abdul-Latiff Z., Othman A.

    Published 2024
    Article
    Save to List
    Saved in:
  5. 5
    Point-of-care Quantitative Measure Of G6pd Enzyme Activity

    Point-of-care Quantitative Measure Of G6pd Enzyme Activity by Darnina A.J., Azlin I., Azma R.Z., Alina M.F., Mimi-Azura A., Cheah F.C., Nazarudin S., Najiah-Ajlaa A., Malisa M.Y., Norunaluwar J., Ainoon O

    Published 2024
    Article
    Save to List
    Saved in:
  6. 6
    Prevalence of iron deficiency anaemia and thalassaemia trait among undergraduate medical students

    Prevalence of iron deficiency anaemia and thalassaemia trait among undergraduate medical students by Azma R.Z., Ainoon O., Azlin I., Hamenuddin H., Hadi N.A., Tatt W.K., Syazana I.N., Asmaliza A.M., Das S., Hamidah N.H.

    Published 2024
    Article
    Save to List
    Saved in:
  7. 7
    Co-inheritance of compound heterozygous Hb constant spring and a single -α 3.7 gene deletion with heterozygous δβ thalassaemia: A diagnostic challenge

    Co-inheritance of compound heterozygous Hb constant spring and a single -α 3.7 gene deletion with heterozygous δβ thalassaemia: A diagnostic challenge by Azma R.Z., Othman A., Azman N., Alauddin H., Ithnin A., Yusof N., Razak N.F., Sardi N.H., Hussin N.H.

    Published 2024
    journal::journal article
    Save to List
    Saved in:
  8. 8
    Evaluation of Glucose-6-phosphate dehydrogenase stability in stored blood samples

    Evaluation of Glucose-6-phosphate dehydrogenase stability in stored blood samples by Jalil N., Azma R.Z., Mohamed E., Ithnin A., Alauddin H., Baya S.N., Othman A.

    Published 2024
    Article
    Save to List
    Saved in:
  9. 9
    A Unique Interaction of IVS-I-1 (G>A) (HBA2: c.95+1G>A) with Hb Adana (HBA2: c.179G>A) Presenting as Transfusion-Dependent ?-Thalassemia

    A Unique Interaction of IVS-I-1 (G>A) (HBA2: c.95+1G>A) with Hb Adana (HBA2: c.179G>A) Presenting as Transfusion-Dependent ?-Thalassemia by Alauddin H., Kamarudin K., Loong T.Y., Azma R.Z., Ithnin A., Jalil N., Razak N.-F., Koh-Xuan-Rong D., Ismail E., C-Khai L., Abdul Latiff Z., Alias H., Othman A.

    Published 2024
    journal::journal article
    Save to List
    Saved in:
  10. 10
    Molecular characteristic of alpha thalassaemia among patients diagnosed in UKM medical centre

    Molecular characteristic of alpha thalassaemia among patients diagnosed in UKM medical centre by Azma R.Z., Ainoon O., Hafiza A., Azlin I., Noor Farisah A.R., Nor Hidayati S., Noor Hamidah H.

    Published 2024
    Article
    Save to List
    Saved in:
  11. 11
    Genotyping of Malaysian G6PD-deficient neonates by reverse dot blot flow-through hybridisation

    Genotyping of Malaysian G6PD-deficient neonates by reverse dot blot flow-through hybridisation by Alina M.F., Azma R.Z., Norunaluwar J., Azlin I., Darnina A.J., Cheah F.C., Noor-Farisah A.R., Siti-Hawa A.A., Danny X.R.K., Zulkifli N.F., Ainoon O.

    Published 2024
    journal::journal article
    Save to List
    Saved in:

Search Tools: