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H Chui

Showing results (91-100 of 293) with videos related to

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Genomics|April 16, 1998
Electronic access to sequence alignments, experimental results, and human mutations as an aid to studying globin gene regulationR Hardison, C Riemer, D H Chui, et al.
Blood|March 1, 1986
Hemoglobin switching during murine embryonic development: evidence for two populations of embryonic erythropoietic progenitor cellsP M Wong, S W Chung, S M Reicheld, et al.
American Journal of Hematology|December 22, 1999
PCR-based diagnosis of the Filipino (--(FIL)) and Thai (--(THAI)) alpha-thalassemia-1 deletionsB Eng, M Patterson, S Borys, et al.
International Journal of Environmental Research and Public Health|January 2, 2019
Cardiovascular Disease Hospitalizations in Louisiana Parishes' Elderly before, during and after Hurricane KatrinaNinon A Becquart, Elena N Naumova, Gitanjali Singh, et al.
Clinical Chemistry|August 1, 1989
Enzyme-linked immunosorbent assay for free thyroxin in human serumS H Chui, K C Wan, C W Lam, et al.
Journal of Clinical Immunology|July 1, 1991
Light-chain ratio of serum IgA1 in IgA nephropathyS H Chui, C W Lam, W H Lewis, et al.
Blood|April 1, 1988
An immunoassay to detect human embryonic epsilon globin chains by a murine monoclonal antibodyJ Q Zhao, H Y Luo, B J Clarke, et al.
Hemoglobin|July 1, 1997
Novel beta 0-thalassemia mutation in a Canadian woman of British descent (codons 72/73, -AGTGA, +T)J S Waye, B Eng, M Patterson, et al.
Hemoglobin|March 11, 1998
Novel beta-thalassemia mutation in patients of Jewish descent: [beta 30(B12)Arg-->Gly or IVS-I(-2)(A-->G)]J S Waye, B Eng, M Patterson, et al.
Blood|June 1, 1994
Identification of a novel termination codon mutation (TAA-->TAT, Term-->Tyr) in the alpha 2 globin gene of a Laotian girl with hemoglobin H diseaseJ S Waye, B Eng, M Patterson, et al.
Pageof 30

Showing results (91-100 of 293) with videos related to

Sort By:
Pageof 30
Genomics|April 16, 1998
Electronic access to sequence alignments, experimental results, and human mutations as an aid to studying globin gene regulationR Hardison, C Riemer, D H Chui, et al.
Blood|March 1, 1986
Hemoglobin switching during murine embryonic development: evidence for two populations of embryonic erythropoietic progenitor cellsP M Wong, S W Chung, S M Reicheld, et al.
American Journal of Hematology|December 22, 1999
PCR-based diagnosis of the Filipino (--(FIL)) and Thai (--(THAI)) alpha-thalassemia-1 deletionsB Eng, M Patterson, S Borys, et al.
International Journal of Environmental Research and Public Health|January 2, 2019
Cardiovascular Disease Hospitalizations in Louisiana Parishes' Elderly before, during and after Hurricane KatrinaNinon A Becquart, Elena N Naumova, Gitanjali Singh, et al.
Clinical Chemistry|August 1, 1989
Enzyme-linked immunosorbent assay for free thyroxin in human serumS H Chui, K C Wan, C W Lam, et al.
Journal of Clinical Immunology|July 1, 1991
Light-chain ratio of serum IgA1 in IgA nephropathyS H Chui, C W Lam, W H Lewis, et al.
Blood|April 1, 1988
An immunoassay to detect human embryonic epsilon globin chains by a murine monoclonal antibodyJ Q Zhao, H Y Luo, B J Clarke, et al.
Hemoglobin|July 1, 1997
Novel beta 0-thalassemia mutation in a Canadian woman of British descent (codons 72/73, -AGTGA, +T)J S Waye, B Eng, M Patterson, et al.
Hemoglobin|March 11, 1998
Novel beta-thalassemia mutation in patients of Jewish descent: [beta 30(B12)Arg-->Gly or IVS-I(-2)(A-->G)]J S Waye, B Eng, M Patterson, et al.
Blood|June 1, 1994
Identification of a novel termination codon mutation (TAA-->TAT, Term-->Tyr) in the alpha 2 globin gene of a Laotian girl with hemoglobin H diseaseJ S Waye, B Eng, M Patterson, et al.
Pageof 30