N. Razak

发表

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

H. Alias, A. Othman, A. Ithnin, 2014, Hemoglobin.

Co-inheritance of compound heterozygous Hb Constant Spring and a single -alpha(3.7) gene deletion with heterozygous deltabeta thalassaemia: a diagnostic challenge.

N. Hussin, A. Othman, A. Ithnin, 2012, The Malaysian journal of pathology.

Multiplex STR panel for assessment of chimerism following hematopoietic stem cell transplantation (HSCT)

N. Hussin, R. Hassan, A. Othman, 2019, Annals of Hematology.

FISH versus real-time quantitative PCR for monitoring of minimal residual disease in chronic myeloid leukaemia patients on tyrosine kinase inhibitor therapy.

A. Tamil, S. Shuib, A. Ithnin, 2019, The Malaysian journal of pathology.