Search Results - Loh C.-K.

Hb lepore/β0-thalassaemia with α+-thalassaemia interactions, a potential diagnostic pitfall by Alauddin H., Mohamad Nasir S., Ahadon M., Raja Sabudin R.Z.A., Ithnin A., Hussin N.H., Alias H., Loh C.-K., Abdul Latiff Z., Abdul Murad N.A., Othman A.

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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.