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Showing results (271-280 of 355) with videos related to

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Human Genetics|May 1, 1992
Human alpha-globin gene expression is silenced by terminal truncation of chromosome 16p beginning immediately 3' of the zeta-globin geneL Romao, F Cash, I Weiss, et al.
Hemoglobin|January 1, 1988
Homozygous beta zero-39 mutation with thalassemia intermedia in northern Sardinia: clinical, hematological and molecular analysisL Oggiano, F Dore, P Pistidda, et al.
Human Genetics|January 1, 1988
Beta-thalassemia mutations in the Portuguese populationM P Gomes, M G da Costa, L B Braga, et al.
Archives of Disease in Childhood|March 1, 1988
Depletion of trace elements and acute ocular toxicity induced by desferrioxamine in patients with thalassaemiaS De Virgiliis, M Congia, M P Turco, et al.
Tissue Antigens|May 1, 1992
The HLA DQB1*0502 allele is neutrally associated with insulin-dependent diabetes mellitus in the Sardinian populationF Muntoni, M Congia, F Cucca, et al.
Genomics|October 27, 1997
Analysis of exon/intron structure and 400 kb of genomic sequence surrounding the 5'-promoter and 3'-terminal ends of the human glypican 3 (GPC3) geneR Huber, L Crisponi, R Mazzarella, et al.
British Journal of Haematology|December 31, 1997
Hyperbilirubinaemia in heterozygous beta-thalassaemia is related to co-inherited Gilbert's syndromeR Galanello, L Perseu, M A Melis, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1993
Dystrophin analysis using a panel of anti-dystrophin antibodies in Duchenne and Becker muscular dystrophyF Muntoni, A Mateddu, C Cianchetti, et al.
Clinical Journal of the American Society of Nephrology : CJASN|October 3, 2015
Risk Stratification for Rejection and Infection after Kidney TransplantationPietro E Cippà, Marc Schiesser, Henrik Ekberg, et al.
British Journal of Haematology|November 1, 1982
The interaction of alpha thalassaemia with heterozygous beta thalassaemiaE Kanavakis, J S Wainscoat, W G Wood, et al.
Pageof 36

Showing results (271-280 of 355) with videos related to

Sort By:
Pageof 36
Human Genetics|May 1, 1992
Human alpha-globin gene expression is silenced by terminal truncation of chromosome 16p beginning immediately 3' of the zeta-globin geneL Romao, F Cash, I Weiss, et al.
Hemoglobin|January 1, 1988
Homozygous beta zero-39 mutation with thalassemia intermedia in northern Sardinia: clinical, hematological and molecular analysisL Oggiano, F Dore, P Pistidda, et al.
Human Genetics|January 1, 1988
Beta-thalassemia mutations in the Portuguese populationM P Gomes, M G da Costa, L B Braga, et al.
Archives of Disease in Childhood|March 1, 1988
Depletion of trace elements and acute ocular toxicity induced by desferrioxamine in patients with thalassaemiaS De Virgiliis, M Congia, M P Turco, et al.
Tissue Antigens|May 1, 1992
The HLA DQB1*0502 allele is neutrally associated with insulin-dependent diabetes mellitus in the Sardinian populationF Muntoni, M Congia, F Cucca, et al.
Genomics|October 27, 1997
Analysis of exon/intron structure and 400 kb of genomic sequence surrounding the 5'-promoter and 3'-terminal ends of the human glypican 3 (GPC3) geneR Huber, L Crisponi, R Mazzarella, et al.
British Journal of Haematology|December 31, 1997
Hyperbilirubinaemia in heterozygous beta-thalassaemia is related to co-inherited Gilbert's syndromeR Galanello, L Perseu, M A Melis, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1993
Dystrophin analysis using a panel of anti-dystrophin antibodies in Duchenne and Becker muscular dystrophyF Muntoni, A Mateddu, C Cianchetti, et al.
Clinical Journal of the American Society of Nephrology : CJASN|October 3, 2015
Risk Stratification for Rejection and Infection after Kidney TransplantationPietro E Cippà, Marc Schiesser, Henrik Ekberg, et al.
British Journal of Haematology|November 1, 1982
The interaction of alpha thalassaemia with heterozygous beta thalassaemiaE Kanavakis, J S Wainscoat, W G Wood, et al.
Pageof 36