Results 21 to 40 of 41
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TypeTitleAuthor(s)YearViews
Thalassemia screening based on red cell indices in the ChineseMa, ESK; Chan, AYY; Yin Ha, S; Lau, YL; Chan, LC2001133
 
Interaction between (-SEA) α-thalassemla deletion and uncommon non-deletional α-globin gene mutations in Chinese patientsMa, ESK; De Chow, EY; Chan, AYY; Chan, LC200160
 
A novel AATAAA→CATAAA mutation at the polyadenylation site of the β-globin gene [3]Ma, SK; Lee, ACW; Chan, AYY; Chan, LC200155
 
Haemoglobin Q-Thailand and hereditary spherocytosis in a chinese familyLeung, KFS; Au, WY; Chan, AYY; Chan, LC; Waye, JS; Chui, DHK; Ma, SK2001122
 
Should we screen for globin gene mutations in blood samples with mean corpuscular volume (MCV) greater than 80 fL in areas with a high prevalence of thalassaemia?Chan, LC; Ma, SK; Chan, AYY; Ha, SY; Waye, JS; Lau, YL; Chui, DHK2001312
 
Haemoglobin H disease due to (--SEA) α-globin gene deletion and α2-codon 30 (ΔGAG) mutation: A family studyMa, SK; Chan, AYY; Chiu, EKW; Chan, LC200185
 
Screening for (-(SEA)) α-globin gene deletion in β-thalassemia carriers and prevention of hydrops fetalisMa, ESK; Chan, AYY; Shau Yin Ha; Chan, GCF; Yu Lung Lau; Li Chong Chan200070
 
Thalassaemia Screening in Hong Kong Strategies and Potential PitfallsMa, ESK; Chan, AYY; Ha, SY; Chan, GCF; Lau, YL; Chan, LC200067
 
Screening of a-thalassemia in b-thalassemia Carriers and Prevention of Hydrops FetailsMa, ESK; Chan, AYY; Ha, SY; Chan, GCF; Lau, YL; Chan, LC200072
 
Compound heterozygosity for triplicated α-globin gene and (- -(SEA)) α-globin gene deletion: Implication for thalassaemia screening [5]Ma, SK; Chan, AYY; Chan, LC; Chui, DHK; Waye, JS200061
 
Two novel β-thalassemia alleles in the chinese: The IVS-II-2 (-T) and nucleotide +8 (C→T) β-globin gene mutationsMa, SK; Ha, SY; Chan, AYY; Chan, GCF; Lau, YL; Chan, LC200058
 
β-Thalassemia intermedia caused by compound heterozygosity for Hb Malay (β codon 19 AAC→AGC; Asn→Ser) and codons 41/42 (-CTTT) β0-thalassemia mutationMa, SK; Chow, EYD; Chan, AYY; Kung, NNS; Waye, JS; Chan, LC; Chui, DHK2000180
 
Two Novel b-thalassemia alleles in the Chinese: IVSII-2(-T) b-Zero Mutation and NT+8 (C - T) Silent b-Plus MutationMa, ESK; Chan, AYY; Ha, SY; Chan, GCF; Chan, LC199969
 
Genotype-phenotype correlation of b-thalassemia patients in Hong KongMa, ESK; Ha, SY; Chan, AYY; Chan, GCF; Chan, LC; Chui, DHK199997
 
Myelodysplastic syndrome with myelofibrosis and basophilia : Detection of trisomy 8 in basophils by fluorescence in-situ hybridizationMa, SK; Chan, JCW; Wan, TSK; Chan, AYY; Chan, LC199897
 
Comparison of the HbH inclusion test and a PCR test in routine screening for α thalassaemia in Hong KongChan, AYY; So, CKC; Chan, LC1996271
 
Inversion (14)(q11q32) in childhood T-cell acute lymphoblastic leukemiaKwong, YL; Shing, MK; Wan, TM; Yuen, PMP; Chan, AYY; Wong, KF; Chan, LC199480
 
Cytogenetic triclonality in acute myeloid leukemia: A morphologic, immunologic and in situ hybridization studyKwong, YL; Lam, CK; Chan, AYY; Lie, AKW; Chan, LC1994103
 
Near-octaploidy in essential thrombocythemiaKwong, YL; Chan, AYY; Wei, D; Chan, LC199359
 
Near-triploid myeloblastic transformation of chronic myeloid leukemia with bizarre blast morphologyKwong, YL; Chan, AYY; Chan, LC; Wong, KF; Chu, YC199279
 
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