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A Cao

Showing results (161-170 of 461) with videos related to

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The Journal of Biological Chemistry|October 25, 1984
Initiation codon mutation as a cause of alpha thalassemiaM Pirastu, G Saglio, J C Chang, et al.
International Journal of Spine Surgery|May 28, 2019
Postoperative Complications Following Orthopedic Spine Surgery: Is There a Difference Between Men and Women?Jessica H Heyer, N A Cao, Richard L Amdur, et al.
The Journal of Clinical Investigation|November 1, 1987
An initiation codon mutation (AUG----GUG) of the human alpha 1-globin gene. Structural characterization and evidence for a mild thalassemic phenotypeP Moi, F E Cash, S A Liebhaber, et al.
Hemoglobin|March 11, 1998
Hb Sassari [alpha 126(H9)Asp-->His] results from a GAC-->CAC mutation in the alpha 1-globin geneE Paglietti, S Barella, S Satta, et al.
Recenti Progressi in Medicina|April 1, 1992
Prenatal diagnosis of inherited hemoglobinopathiesA Cao, G B Leoni, R Sardu, et al.
Journal of Medical Genetics|November 1, 1988
Beta thalassaemia mutations in Turkish CypriotsA Sozuoz, A Berkalp, A Figus, et al.
Hemoglobin|January 1, 1984
Developmental pattern of beta-chain production at midtrimester pregnancy in Sardinian beta o-thalassemia heterozygotesC Rosatelli, A M Falchi, M T Scalas, et al.
BMC Plant Biology|April 29, 2019
Genome-wide association analysis for fumonisin content in maize kernelsL F Samayoa, A Cao, R Santiago, et al.
Haematologica|July 1, 1990
Preliminary experience with the differential pH technique for glucose-6-phosphate dehydrogenase (G6PD) measurement in whole blood: application to an area with high prevalence of thalassaemia and G6PD deficiencyA Mosca, M Paderi, A Sanna, et al.
British Journal of Haematology|October 1, 1987
Molecular characterization of a normal Hb A2 beta-thalassaemia determinant in a Sardinian familyL Oggiano, M Pirastu, P Moi, et al.
Pageof 47

Showing results (161-170 of 461) with videos related to

Sort By:
Pageof 47
The Journal of Biological Chemistry|October 25, 1984
Initiation codon mutation as a cause of alpha thalassemiaM Pirastu, G Saglio, J C Chang, et al.
International Journal of Spine Surgery|May 28, 2019
Postoperative Complications Following Orthopedic Spine Surgery: Is There a Difference Between Men and Women?Jessica H Heyer, N A Cao, Richard L Amdur, et al.
The Journal of Clinical Investigation|November 1, 1987
An initiation codon mutation (AUG----GUG) of the human alpha 1-globin gene. Structural characterization and evidence for a mild thalassemic phenotypeP Moi, F E Cash, S A Liebhaber, et al.
Hemoglobin|March 11, 1998
Hb Sassari [alpha 126(H9)Asp-->His] results from a GAC-->CAC mutation in the alpha 1-globin geneE Paglietti, S Barella, S Satta, et al.
Recenti Progressi in Medicina|April 1, 1992
Prenatal diagnosis of inherited hemoglobinopathiesA Cao, G B Leoni, R Sardu, et al.
Journal of Medical Genetics|November 1, 1988
Beta thalassaemia mutations in Turkish CypriotsA Sozuoz, A Berkalp, A Figus, et al.
Hemoglobin|January 1, 1984
Developmental pattern of beta-chain production at midtrimester pregnancy in Sardinian beta o-thalassemia heterozygotesC Rosatelli, A M Falchi, M T Scalas, et al.
BMC Plant Biology|April 29, 2019
Genome-wide association analysis for fumonisin content in maize kernelsL F Samayoa, A Cao, R Santiago, et al.
Haematologica|July 1, 1990
Preliminary experience with the differential pH technique for glucose-6-phosphate dehydrogenase (G6PD) measurement in whole blood: application to an area with high prevalence of thalassaemia and G6PD deficiencyA Mosca, M Paderi, A Sanna, et al.
British Journal of Haematology|October 1, 1987
Molecular characterization of a normal Hb A2 beta-thalassaemia determinant in a Sardinian familyL Oggiano, M Pirastu, P Moi, et al.
Pageof 47