A novel single gene deletion (-αMAL3.5) giving rise to silent α thalassemia carrier removing the entire HBA2 gene observed in two Chinese patients with Hb H disease: case report of...

by Faidatul Syazlin Abdul Hamid, Rahimah Ahmad, Mohamed Saleem, Nur Aisyah Aziz, Syahira Lazira Omar, Siti Hida Hajira Mohamad Arif, Jameela Sathar, Zubaidah Zakaria
Published 2015-07-01

Evidence of new intragenic HBB haplotypes model for the prediction of beta-thalassemia in the Malaysian population

by Nur-Aisyah Aziz, Wan-Rohani Wan Taib, Nur-Khairunnisa Kharolazaman, Imilia Ismail, Hamid Ali Nagi Al-Jamal, Nadiah Wan-Arfah Wan Abdul Jamil, Ezalia Esa, Hishamshah Ibrahim
Published 2021-08-01