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L F Bernini

Showing results (51-60 of 73) with videos related to

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Annals of Human Genetics|January 1, 1991
Multiple recombination events are responsible for the heterogeneity of alpha(+)-thalassemia haplotypes among the forest tribes of Andhra Pradesh, IndiaR Fodde, C L Harteveld, M Losekoot, et al.
European Journal of Human Genetics : EJHG|April 10, 1999
A complex haemoglobinopathy diagnosis in a family with both beta zero- and alpha (zero/+)-thalassaemia homozygosityP C Giordano, C L Harteveld, L A Bok, et al.
Haematologica|January 9, 2001
Different geographic origins of Hb Constant Spring [alpha(2) codon 142 TAA-->CAA]C L Harteveld, J Traeger-Synodinos, A Ragusa, et al.
Community Genetics|June 5, 2004
The molecular spectrum of beta-thalassemia and abnormal hemoglobins in the allochthonous and autochthonous dutch populationP C Giordano, C L Harteveld, A J Heister, et al.
Biopolymers|November 1, 1996
CD and NMR structural characterization of ceratotoxins, natural peptides with antimicrobial activityL Ragona, H Molinari, L Zetta, et al.
British Journal of Haematology|September 1, 1996
Hb Utrecht [alpha 2 129(H12)Leu-->Pro], a new unstable alpha 2-chain variant associated with a mild alpha-thalassaemic phenotypeC L Harteveld, P C Giordano, M Losekoot, et al.
Blood|February 15, 1991
Interaction of two different disorders in the beta-globin gene cluster associated with an increased hemoglobin F production: a novel deletion type of (G) gamma + ((A) gamma delta beta)(0)-thalassemia and a delta(0)-hereditary persistence of fetal hemoglobin determinantM Losekoot, R Fodde, E J Gerritsen, et al.
American Journal of Hematology|January 1, 1997
Properties of the mouse alpha-globin HS-26: relationship to HS-40, the major enhancer of human alpha-globin gene expressionE E Bouhassira, M F Kielman, J Gilman, et al.
Annals of Hematology|October 1, 1996
Hb Malmö [beta-97(FG-4)His-->Gln] leading to polycythemia in a Dutch familyP C Giordano, C L Harteveld, A Brand, et al.
British Journal of Haematology|November 25, 1998
A case of non-beta-globin gene linked beta thalassaemia in a Dutch family with two additional alpha-gene defects: the common -alpha3.7 deletion and the rare IVS1-116 (A-->G) acceptor splice site mutationP C Giordano, C L Harteveld, H L Haak, et al.
Pageof 8

Showing results (51-60 of 73) with videos related to

Sort By:
Pageof 8
Annals of Human Genetics|January 1, 1991
Multiple recombination events are responsible for the heterogeneity of alpha(+)-thalassemia haplotypes among the forest tribes of Andhra Pradesh, IndiaR Fodde, C L Harteveld, M Losekoot, et al.
European Journal of Human Genetics : EJHG|April 10, 1999
A complex haemoglobinopathy diagnosis in a family with both beta zero- and alpha (zero/+)-thalassaemia homozygosityP C Giordano, C L Harteveld, L A Bok, et al.
Haematologica|January 9, 2001
Different geographic origins of Hb Constant Spring [alpha(2) codon 142 TAA-->CAA]C L Harteveld, J Traeger-Synodinos, A Ragusa, et al.
Community Genetics|June 5, 2004
The molecular spectrum of beta-thalassemia and abnormal hemoglobins in the allochthonous and autochthonous dutch populationP C Giordano, C L Harteveld, A J Heister, et al.
Biopolymers|November 1, 1996
CD and NMR structural characterization of ceratotoxins, natural peptides with antimicrobial activityL Ragona, H Molinari, L Zetta, et al.
British Journal of Haematology|September 1, 1996
Hb Utrecht [alpha 2 129(H12)Leu-->Pro], a new unstable alpha 2-chain variant associated with a mild alpha-thalassaemic phenotypeC L Harteveld, P C Giordano, M Losekoot, et al.
Blood|February 15, 1991
Interaction of two different disorders in the beta-globin gene cluster associated with an increased hemoglobin F production: a novel deletion type of (G) gamma + ((A) gamma delta beta)(0)-thalassemia and a delta(0)-hereditary persistence of fetal hemoglobin determinantM Losekoot, R Fodde, E J Gerritsen, et al.
American Journal of Hematology|January 1, 1997
Properties of the mouse alpha-globin HS-26: relationship to HS-40, the major enhancer of human alpha-globin gene expressionE E Bouhassira, M F Kielman, J Gilman, et al.
Annals of Hematology|October 1, 1996
Hb Malmö [beta-97(FG-4)His-->Gln] leading to polycythemia in a Dutch familyP C Giordano, C L Harteveld, A Brand, et al.
British Journal of Haematology|November 25, 1998
A case of non-beta-globin gene linked beta thalassaemia in a Dutch family with two additional alpha-gene defects: the common -alpha3.7 deletion and the rare IVS1-116 (A-->G) acceptor splice site mutationP C Giordano, C L Harteveld, H L Haak, et al.
Pageof 8