Showing results 1 to 6 of 6
| Title | Author(s) | Issue Date | |
|---|---|---|---|
Compound heterozygosity for triplicated α-globin gene and (- -(SEA)) α-globin gene deletion: Implication for thalassaemia screening [5] Journal:British Journal of Haematology | 2000 | ||
Haemoglobin Q-Thailand and hereditary spherocytosis in a chinese family Journal:Clinical and Laboratory Haematology | 2001 | ||
Hong Kong needs a carrier screening programme for the thalassaemias Proceeding/Conference:Journal of Paediatrics and Child Health | 1997 | ||
Prevalence and genotypes of α- and β-thalassemia carriers in Hong Kong - Implications for population screening Journal:New England Journal of Medicine | 1997 | ||
| 2001 | |||
β-Thalassemia intermedia caused by compound heterozygosity for Hb Malay (β codon 19 AAC→AGC; Asn→Ser) and codons 41/42 (-CTTT) β0-thalassemia mutation Journal:American Journal of Hematology | 2000 |