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D H Chui

Showing results (101-110 of 129) with videos related to

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Hemoglobin|November 24, 1999
Compound heterozygosity for Hb S and Hb G-CopenhagenM D Carcao, L Chang, A Poon, et al.
Human Mutation|January 1, 1994
Hb FM-Fort Ripley: confirmation of autosomal dominant inheritance and diagnosis by PCR and direct nucleotide sequencingR D Hain, D Chitayat, R Cooper, et al.
Blood|December 1, 1983
Adult hemoglobins are synthesized in murine fetal hepatic erythropoietic cellsP M Wong, S W Chung, J S White, et al.
The Journal of Clinical Investigation|June 8, 2000
Hla-DR2-restricted responses to proteolipid protein 95-116 peptide cause autoimmune encephalitis in transgenic miceK Kawamura, T Yamamura, K Yokoyama, et al.
Blood|March 1, 1992
Two novel beta-thalassemia mutations in the 5' and 3' noncoding regions of the beta-globin geneS P Cai, B Eng, W H Francombe, et al.
American Journal of Hematology|October 1, 1991
Hb S/beta zero-thalassemia due to the approximately 1.4-kb deletion is associated with a relatively mild phenotypeJ S Waye, D H Chui, B Eng, et al.
American Journal of Hematology|June 22, 2000
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 mutationS K Ma, E Y Chow, A Y Chan, et al.
Journal of Clinical Pathology|April 18, 2001
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?L C Chan, S K Ma, A Y Chan, et al.
The New England Journal of Medicine|May 1, 1997
Prevalence and genotypes of alpha- and beta-thalassemia carriers in Hong Kong -- implications for population screeningY L Lau, L C Chan, Y Y Chan, et al.
Progress in Clinical and Biological Research|January 1, 1978
Alterations in erythrocyte membrane material properties: a marker of the membrane abnormality in human and chicken muscular dystrophyY F Missirlis, I L Kohn, J D Vickers, et al.
Pageof 13

Showing results (101-110 of 129) with videos related to

Sort By:
Pageof 13
Hemoglobin|November 24, 1999
Compound heterozygosity for Hb S and Hb G-CopenhagenM D Carcao, L Chang, A Poon, et al.
Human Mutation|January 1, 1994
Hb FM-Fort Ripley: confirmation of autosomal dominant inheritance and diagnosis by PCR and direct nucleotide sequencingR D Hain, D Chitayat, R Cooper, et al.
Blood|December 1, 1983
Adult hemoglobins are synthesized in murine fetal hepatic erythropoietic cellsP M Wong, S W Chung, J S White, et al.
The Journal of Clinical Investigation|June 8, 2000
Hla-DR2-restricted responses to proteolipid protein 95-116 peptide cause autoimmune encephalitis in transgenic miceK Kawamura, T Yamamura, K Yokoyama, et al.
Blood|March 1, 1992
Two novel beta-thalassemia mutations in the 5' and 3' noncoding regions of the beta-globin geneS P Cai, B Eng, W H Francombe, et al.
American Journal of Hematology|October 1, 1991
Hb S/beta zero-thalassemia due to the approximately 1.4-kb deletion is associated with a relatively mild phenotypeJ S Waye, D H Chui, B Eng, et al.
American Journal of Hematology|June 22, 2000
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 mutationS K Ma, E Y Chow, A Y Chan, et al.
Journal of Clinical Pathology|April 18, 2001
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?L C Chan, S K Ma, A Y Chan, et al.
The New England Journal of Medicine|May 1, 1997
Prevalence and genotypes of alpha- and beta-thalassemia carriers in Hong Kong -- implications for population screeningY L Lau, L C Chan, Y Y Chan, et al.
Progress in Clinical and Biological Research|January 1, 1978
Alterations in erythrocyte membrane material properties: a marker of the membrane abnormality in human and chicken muscular dystrophyY F Missirlis, I L Kohn, J D Vickers, et al.
Pageof 13