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L F Bernini

Showing results (31-40 of 73) with videos related to

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Clinical and Laboratory Haematology|December 3, 1999
Haemoglobinopathy analyses in the Netherlands: a report of an in vitro globin chain biosynthesis survey using a rapid, modified methodP C Giordano, P Van Delft, D Batelaan, et al.
Human Genetics|January 1, 1985
Molecular evidence of triplication in the haptoglobin Johnson variant geneS Oliviero, M DeMarchi, A O Carbonara, et al.
Human Mutation|January 1, 1996
Rapid detection of point mutations and polymorphisms of the alpha-globin genes by DGGE and SSCAK L Harteveld, A J Heister, P C Giordano, et al.
British Journal of Haematology|October 1, 1990
Denaturing gradient gel electrophoresis and direct sequencing of PCR amplified genomic DNA: a rapid and reliable diagnostic approach to beta thalassaemiaM Losekoot, R Fodde, C L Harteveld, et al.
Haematologica|September 1, 1992
Hemoglobin Sabine [beta 91 (F7) Leu-->Pro]: occurrence in a Sardinian individual with hemolytic anemia and inclusion bodiesD Gasperini, R Galanello, M A Melis, et al.
Journal of Medical Genetics|June 1, 1982
Delta beta (F)-thalassaemia in SardiniaA Cao, M A Melis, R Galanello, et al.
Hemoglobin|November 24, 1999
Hb Aghia Sophia [alpha62(E11)Val-->0 (alpha1)], an "in-frame" deletion causing alpha-thalassemiaJ Traeger-Synodinos, C L Harteveld, E Kanavakis, et al.
British Journal of Haematology|September 21, 2000
alpha-thalassaemia as a result of a novel splice donor site mutation of the alpha1-globin geneC L Harteveld, C Beijer, P van Delft, et al.
British Journal of Haematology|May 1, 1994
A novel polyadenylation signal mutation in the alpha 2-globin gene causing alpha thalassaemiaC L Harteveld, M Losekoot, H Haak, et al.
Journal of Immunogenetics|August 1, 1979
Genetic control of survival in epidemicsR R de Vries, P Meera Khan, L F Bernini, et al.
Pageof 8

Showing results (31-40 of 73) with videos related to

Sort By:
Pageof 8
Clinical and Laboratory Haematology|December 3, 1999
Haemoglobinopathy analyses in the Netherlands: a report of an in vitro globin chain biosynthesis survey using a rapid, modified methodP C Giordano, P Van Delft, D Batelaan, et al.
Human Genetics|January 1, 1985
Molecular evidence of triplication in the haptoglobin Johnson variant geneS Oliviero, M DeMarchi, A O Carbonara, et al.
Human Mutation|January 1, 1996
Rapid detection of point mutations and polymorphisms of the alpha-globin genes by DGGE and SSCAK L Harteveld, A J Heister, P C Giordano, et al.
British Journal of Haematology|October 1, 1990
Denaturing gradient gel electrophoresis and direct sequencing of PCR amplified genomic DNA: a rapid and reliable diagnostic approach to beta thalassaemiaM Losekoot, R Fodde, C L Harteveld, et al.
Haematologica|September 1, 1992
Hemoglobin Sabine [beta 91 (F7) Leu-->Pro]: occurrence in a Sardinian individual with hemolytic anemia and inclusion bodiesD Gasperini, R Galanello, M A Melis, et al.
Journal of Medical Genetics|June 1, 1982
Delta beta (F)-thalassaemia in SardiniaA Cao, M A Melis, R Galanello, et al.
Hemoglobin|November 24, 1999
Hb Aghia Sophia [alpha62(E11)Val-->0 (alpha1)], an "in-frame" deletion causing alpha-thalassemiaJ Traeger-Synodinos, C L Harteveld, E Kanavakis, et al.
British Journal of Haematology|September 21, 2000
alpha-thalassaemia as a result of a novel splice donor site mutation of the alpha1-globin geneC L Harteveld, C Beijer, P van Delft, et al.
British Journal of Haematology|May 1, 1994
A novel polyadenylation signal mutation in the alpha 2-globin gene causing alpha thalassaemiaC L Harteveld, M Losekoot, H Haak, et al.
Journal of Immunogenetics|August 1, 1979
Genetic control of survival in epidemicsR R de Vries, P Meera Khan, L F Bernini, et al.
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