Rahimah B. Ahmad
Kuala Lumpur, 50588, Malaysia
Last Updated: 09/26/2026
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Found 8 publications
Rare cause of transfusion-dependent hemolytic anemia: A case report of HbE/Hb Nottingham and literature review.
Journal: Pediatric blood & cancer
Published: November 12, 2021
Prevalence of 3.7 and 4.2 deletions in Sudanese patients with red cells hypochromia and microcytosis.
Journal: BMC research notes
Published: December 27, 2019
Molecular Characterisation of α- and β-Thalassaemia among Indigenous Senoi Orang Asli Communities in Peninsular Malaysia.
Journal: Annals of human genetics
Published: August 16, 2016
Multiplex amplification refractory mutation system (MARMS) for the detection of β-globin gene mutations among the transfusion-dependent β-thalassemia Malay patients in Kelantan, Northeast of Peninsular Malaysia.
Journal: American journal of blood research
Published: July 07, 2014
Molecular characterization of α- and β-thalassaemia among Malay patients.
Journal: International journal of molecular sciences
Published: February 11, 2014
Distribution of alpha thalassaemia gene variants in diverse ethnic populations in malaysia: data from the institute for medical research.
Journal: International journal of molecular sciences
Published: June 27, 2013
Detection of β-globin Gene Mutations Among β-thalassaemia Carriers and Patients in Malaysia: Application of Multiplex Amplification Refractory Mutation System-Polymerase Chain Reaction.
Journal: The Malaysian journal of medical sciences : MJMS
Published: May 09, 2012
Showing 1-8 of 8
Last Updated: 09/26/2026