• 272 Citations
  • 9 h-Index
20012018
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Fingerprint Dive into the research topics where Zarina Abdul Latiff is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 17 Similar Profiles
Thalassemia Medicine & Life Sciences
Mutation Medicine & Life Sciences
Malaysia Medicine & Life Sciences
Leukemia Medicine & Life Sciences
Pediatrics Medicine & Life Sciences
Severe Combined Immunodeficiency Medicine & Life Sciences
beta-Thalassemia Medicine & Life Sciences
Precursor Cell Lymphoblastic Leukemia-Lymphoma Medicine & Life Sciences

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Research Output 2001 2018

  • 272 Citations
  • 9 h-Index
  • 48 Article

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 α-Thalassemia

Alauddin, H., Kamarudin, K., Tang, Y. L., Raja Sabudin, R. Z. A., Ithnin, A., Jalil, N., Razak, N. F., Koh-Xuan-Rong, D., Ismail, E., Loh, C-K., Abdul Latiff, Z., Alias, H. & Othman, A., 4 Jul 2018, In : Hemoglobin. 42, 4, p. 247-251 5 p.

Research output: Contribution to journalArticle

Thalassemia
Hemoglobins
Mutation
Erythrocyte Indices
RNA Splice Sites
1 Citation (Scopus)

Genetic modifiers of fetal haemoglobin (HbF) and phenotypic severity in β-thalassemia patients

Razak, S. A. A., Abdul Murad, N. A., Masra, F., Chong, D. L. S., Abdullah @ Muda, N., Jalil, N., Alauddin, H., Raja Sabudin, R. Z. A., Ithnin, A., Khai, L. C., Aziz, N. A., Muda, Z., Ibrahim, H. & Abdul Latiff, Z., 1 Jan 2018, In : Current Molecular Medicine. 18, 5, p. 295-305 11 p.

Research output: Contribution to journalArticle

Fetal Hemoglobin
Thalassemia
Polymorphism
Mutation
Multiplex Polymerase Chain Reaction

Genotype-phenotype correlation among Malaysian patients with osteogenesis imperfecta

Mohd Nawawi, N., Selveindran, N. M., Rasat, R., Yock Ping, C., Abdul Latiff, Z., Syed Zakaria, S. Z., A. Jamal, A. R., Abdul Murad, N. A. & Abd Aziz, B. B., 1 Sep 2018, In : Clinica Chimica Acta. 484, p. 141-147 7 p.

Research output: Contribution to journalArticle

Osteogenesis Imperfecta
Genetic Association Studies
Genes
Mutation
Bone

Duplication 17p11.2 (Potocki-Lupski syndrome) in a child with developmental delay

Shuib, S., Saaid, N. N., Zakaria, Z., Ismail, J. & Abdul Latiff, Z., 1 Apr 2017, In : Malaysian Journal of Pathology. 39, 1, p. 77-81 5 p.

Research output: Contribution to journalArticle

Fluorescence In Situ Hybridization
Chromosomes
Chromosome Duplication
Cardiovascular Abnormalities
Muscle Hypotonia
5 Citations (Scopus)

Family history of early infant death correlates with earlier age at diagnosis but not shorter time to diagnosis for severe combined immunodeficiency

Wai Luk, A. D., Lee, P. P., Mao, H., Chan, K. W., Chen, X. Y., Chen, T. X., He, J. X., Kechout, N., Suri, D., Tao, Y. B., Xu, Y. B., Jiang, L. P., Liew, W. K., Jirapongsananuruk, O., Daengsuwan, T., Gupta, A., Singh, S., Rawat, A., Latiff, A. H. A., Lee, A. C. W. & 25 others, Shek, L. P., Nguyen, T. V. A., Chin, T. J., Chien, Y. H., Abdul Latiff, Z., Le, T. M. H., Le, N. N. Q., Lee, B. W., Li, Q., Raj, D., Barbouche, M. R., Thong, M. K., Ang, M. C. D., Wang, X. C., Xu, C. G., Yu, H. G., Yu, H. H., Lee, T. L., Yau, F. Y. S., Wong, W. H. S., Tu, W., Yang, W., Chong, P. C. Y., Ho, M. H. K. & Lau, Y. L., 12 Jul 2017, In : Frontiers in Immunology. 8, JUL, 808.

Research output: Contribution to journalArticle

Severe Combined Immunodeficiency
Mutation
Candidiasis
Bacillus
Infection