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Results: 1-12 |
Results: 12
Clinical phenotype of triplicated alpha-globin genes and heterozygosity for beta(0)-thalassemia in Chinese subjects
Authors: Ma, SK Au, WY Chan, AYY Chan, LC
Citation: Sk. Ma et al., Clinical phenotype of triplicated alpha-globin genes and heterozygosity for beta(0)-thalassemia in Chinese subjects, INT J MOL M, 8(2), 2001, pp. 171-175
Interaction between (--(SEA)) alpha-thalassemia deletion and uncommon non-deletional alpha-globin gene mutations in Chinese patients
Authors: Ma, ESK De Chow, EY Chan, AYY Chan, LC
Citation: Esk. Ma et al., Interaction between (--(SEA)) alpha-thalassemia deletion and uncommon non-deletional alpha-globin gene mutations in Chinese patients, HAEMATOLOG, 86(5), 2001, pp. 539-540
Diagnosis of concurrent hemoglobin H disease and heterozygous beta-thalassemia
Authors: Ma, ESK Chan, AYY Au, WY Yeung, YM Chan, LC
Citation: Esk. Ma et al., Diagnosis of concurrent hemoglobin H disease and heterozygous beta-thalassemia, HAEMATOLOG, 86(4), 2001, pp. 432-433
Thalassemia screening based on red cell indices in the Chinese
Authors: Ma, ESK Chan, AYY Ha, SY Lau, YL Chan, LC
Citation: Esk. Ma et al., Thalassemia screening based on red cell indices in the Chinese, HAEMATOLOG, 86(12), 2001, pp. 1310-1311
Haemoglobin H disease due to (--(SEA)) alpha-globin gene deletion and alpha 2-codon 30 (Delta GAG) mutation: a family study
Authors: Ma, SK Chan, AYY Chiu, EKW Chan, LC
Citation: Sk. Ma et al., Haemoglobin H disease due to (--(SEA)) alpha-globin gene deletion and alpha 2-codon 30 (Delta GAG) mutation: a family study, CLIN LAB H, 23(5), 2001, pp. 325-327
Haemoglobin Q-Thailand and hereditary spherocytosis in a Chinese family
Authors: Leung, KFS Au, WY Chan, AYY Chan, LC Waye, JS Chui, DHK Ma, SK
Citation: Kfs. Leung et al., Haemoglobin Q-Thailand and hereditary spherocytosis in a Chinese family, CLIN LAB H, 23(1), 2001, pp. 53-55
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?
Authors: Chan, LC Ma, SK Chan, AYY Ha, SY Waye, JS Lau, YL Chui, DHK
Citation: Lc. Chan et al., 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?, J CLIN PATH, 54(4), 2001, pp. 317-320
A novel (A)under-barATAAA ->(C)under-barATAAA mutation at the polyadenylation site of the beta-globin gene
Authors: Ma, SK Lee, ACW Chan, AYY Chan, LC
Citation: Sk. Ma et al., A novel (A)under-barATAAA ->(C)under-barATAAA mutation at the polyadenylation site of the beta-globin gene, BR J HAEM, 115(1), 2001, pp. 230-231
Two novel beta-thalassemia alleles in the Chinese: the IVS-II-2 (-T) and nucleotide +8 (C -> T) beta-globin gene mutations
Authors: Ma, SK Ha, SY Chan, AYY Chan, GCF Lau, YL Chan, LC
Citation: Sk. Ma et al., Two novel beta-thalassemia alleles in the Chinese: the IVS-II-2 (-T) and nucleotide +8 (C -> T) beta-globin gene mutations, HEMOGLOBIN, 24(4), 2000, pp. 327-332
beta-thalassemia intermedia caused by compound heterozygosity for Hb Malay(beta codon 19 AAC -> AGC; Asn -> Ser) and codons 41/42 (-CTTT) beta(0)-thalassemia mutation
Authors: Ma, SK Chow, EYD Chan, AYY Kung, NNS Waye, JS Chan, LC Chui, DHK
Citation: Sk. Ma et al., beta-thalassemia intermedia caused by compound heterozygosity for Hb Malay(beta codon 19 AAC -> AGC; Asn -> Ser) and codons 41/42 (-CTTT) beta(0)-thalassemia mutation, AM J HEMAT, 64(3), 2000, pp. 206-209
Compound heterozygosity for triplicated alpha-globin gene and (- -(SEA)) alpha-globin gene deletion: Implication for thalassaemia screening
Authors: Ma, SK Chan, AYY Chan, LC Chui, DHK Waye, JS
Citation: Sk. Ma et al., Compound heterozygosity for triplicated alpha-globin gene and (- -(SEA)) alpha-globin gene deletion: Implication for thalassaemia screening, BR J HAEM, 110(2), 2000, pp. 498-499
Myelodysplastic syndrome with myelofibrosis and basophilia: Detection of trisomy 8 in basophils by fluorescence in-situ hybridization
Authors: Ma, SK Chan, JCW Wan, TSK Chan, AYY Chan, LC
Citation: Sk. Ma et al., Myelodysplastic syndrome with myelofibrosis and basophilia: Detection of trisomy 8 in basophils by fluorescence in-situ hybridization, LEUK LYMPH, 31(3-4), 1998, pp. 429
Risultati: 1-12 |