Showing results 13 to 21 of 21
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Title | Author(s) | Issue Date | |
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Prenatal detection of Hb Barts Disease in Maternal Blood Proceeding/Conference:International Conference on Prenatal Diagnosis & Therapy, ISPD 2004 | 2004 | ||
Prevalence and genotypes of α- and β-thalassemia carriers in Hong Kong - Implications for population screening Journal:New England Journal of Medicine | 1997 | ||
2002 | |||
2001 | |||
Sickle cell disease caused by heterozygosity for Hb S and novel LCR deletion: Report of two patients Journal:American Journal of Hematology | 2009 | ||
2005 | |||
Single-tube multiplex-PCR screen for anti-3.7 and anti-4.2 α-globin gene triplications Journal:Clinical Chemistry | 2003 | ||
Variation and heritability of Hb F and F-cells among β-thalassemia heterozygotes in Hong Kong Journal:American Journal of Hematology | 2008 | ||
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 |