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H F Harris

Showing results (11-20 of 18) with videos related to

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Human Genetics|May 1, 1991
The frequencies of Hbs S and C in Georgia and South CarolinaT H Huisman, H F Harris, A Stewart, et al.
Hemoglobin|January 1, 1978
Hb Suresnes or alpha2 141(HC3) ArgyieldHis beta2 in a black familyM E Gravely, H F Harris, M Stallings, et al.
Biochimica Et Biophysica Acta|September 21, 1989
Hb A2-Wrens or alpha 2 delta 2 98(FG5) Val----Met, an unstable delta chain variant identified by sequence analysis of amplified DNAJ F Codrington, F Kutlar, H F Harris, et al.
American Journal of Human Genetics|November 1, 1983
The Atlanta family with hemoglobin Grady revisitedM P Cleek, M B Gardiner, A L Reese, et al.
Hemoglobin|January 1, 1979
The synthesis of fetal hemoglobin types in red blood cells and in BFU-E derived colonies from peripheral blood of patients with sickle cell anemia, beta+ - and delta beta-thalassemia, various forms of hereditary persistence of fetal hemoglobin, normal adults and newbornT H Huisman, G D Efremov, A L Reese, et al.
American Journal of Hematology|January 1, 1979
The association of sickle cell anemia with heterozygous and homozygous alpha-thalassemia-2: in vitro HB chain synthesisA E Felice, B Webber, A Miller, et al.
Hemoglobin|January 1, 1989
A search for anomalies in the zeta, alpha, beta, and gamma globin gene arrangements in normal black, Italian, Turkish, and Spanish newbornsY J Fei, F Kutlar, H F Harris, et al.
Hemoglobin|January 1, 1980
Hemoglobinopathies observed in the population of the Southeastern United States (SE-USA)T H Huisman, B L Abraham, H F Harris, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Human Genetics|May 1, 1991
The frequencies of Hbs S and C in Georgia and South CarolinaT H Huisman, H F Harris, A Stewart, et al.
Hemoglobin|January 1, 1978
Hb Suresnes or alpha2 141(HC3) ArgyieldHis beta2 in a black familyM E Gravely, H F Harris, M Stallings, et al.
Biochimica Et Biophysica Acta|September 21, 1989
Hb A2-Wrens or alpha 2 delta 2 98(FG5) Val----Met, an unstable delta chain variant identified by sequence analysis of amplified DNAJ F Codrington, F Kutlar, H F Harris, et al.
American Journal of Human Genetics|November 1, 1983
The Atlanta family with hemoglobin Grady revisitedM P Cleek, M B Gardiner, A L Reese, et al.
Hemoglobin|January 1, 1979
The synthesis of fetal hemoglobin types in red blood cells and in BFU-E derived colonies from peripheral blood of patients with sickle cell anemia, beta+ - and delta beta-thalassemia, various forms of hereditary persistence of fetal hemoglobin, normal adults and newbornT H Huisman, G D Efremov, A L Reese, et al.
American Journal of Hematology|January 1, 1979
The association of sickle cell anemia with heterozygous and homozygous alpha-thalassemia-2: in vitro HB chain synthesisA E Felice, B Webber, A Miller, et al.
Hemoglobin|January 1, 1989
A search for anomalies in the zeta, alpha, beta, and gamma globin gene arrangements in normal black, Italian, Turkish, and Spanish newbornsY J Fei, F Kutlar, H F Harris, et al.
Hemoglobin|January 1, 1980
Hemoglobinopathies observed in the population of the Southeastern United States (SE-USA)T H Huisman, B L Abraham, H F Harris, et al.
Pageof 2