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C L Harteveld

Showing results (1-10 of 42) with videos related to

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International Journal of Laboratory Hematology|June 1, 2013
State of the art and new developments in molecular diagnostics for hemoglobinopathies in multiethnic societiesC L Harteveld
Nederlands Tijdschrift Voor Geneeskunde|October 25, 2006
[Prevention of hereditary haemoglobinopathies in The Netherlands]P C Giordano, C L Harteveld
Bailliere'S Clinical Haematology|June 29, 2000
Alpha-thalassaemiaL F Bernini, C L Harteveld
ISRN Hematology|November 16, 2011
Iron depletion: an ameliorating factor for sickle cell disease?P C Giordano, W Huisman, C L Harteveld
Clinical Biochemistry|July 13, 2010
Newborn screening for hemoglobinopathies using capillary electrophoresis technology: Testing the Capillarys Neonat Fast Hb deviceE Mantikou, C L Harteveld, P C Giordano
Acta Clinica Belgica|August 12, 2014
Aberrant glycated haemoglobin (HbA1c) results leading to haemoglobinopathy diagnosis in four Belgian patientsC Van Laer, C L Harteveld, S Pauwels, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|December 1, 1996
Characterization and localization of the mProx1 gene directly upstream of the mouse alpha-globin gene cluster: identification of a polymorphic direct repeat in the 5'UTRM F Kielman, S Barradeau, R Smits, et al.
Hemoglobin|April 13, 2001
Molecular spectrum of beta-thalassemia in the Iranian Province of HormozganM Yavarian, C L Harteveld, D Batelaan, et al.
Blood Cells, Molecules & Diseases|February 6, 2008
Segmental duplications involving the alpha-globin gene cluster are causing beta-thalassemia intermedia phenotypes in beta-thalassemia heterozygous patientsC L Harteveld, C Refaldi, E Cassinerio, et al.
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.
Pageof 5

Showing results (1-10 of 42) with videos related to

Sort By:
Pageof 5
International Journal of Laboratory Hematology|June 1, 2013
State of the art and new developments in molecular diagnostics for hemoglobinopathies in multiethnic societiesC L Harteveld
Nederlands Tijdschrift Voor Geneeskunde|October 25, 2006
[Prevention of hereditary haemoglobinopathies in The Netherlands]P C Giordano, C L Harteveld
Bailliere'S Clinical Haematology|June 29, 2000
Alpha-thalassaemiaL F Bernini, C L Harteveld
ISRN Hematology|November 16, 2011
Iron depletion: an ameliorating factor for sickle cell disease?P C Giordano, W Huisman, C L Harteveld
Clinical Biochemistry|July 13, 2010
Newborn screening for hemoglobinopathies using capillary electrophoresis technology: Testing the Capillarys Neonat Fast Hb deviceE Mantikou, C L Harteveld, P C Giordano
Acta Clinica Belgica|August 12, 2014
Aberrant glycated haemoglobin (HbA1c) results leading to haemoglobinopathy diagnosis in four Belgian patientsC Van Laer, C L Harteveld, S Pauwels, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|December 1, 1996
Characterization and localization of the mProx1 gene directly upstream of the mouse alpha-globin gene cluster: identification of a polymorphic direct repeat in the 5'UTRM F Kielman, S Barradeau, R Smits, et al.
Hemoglobin|April 13, 2001
Molecular spectrum of beta-thalassemia in the Iranian Province of HormozganM Yavarian, C L Harteveld, D Batelaan, et al.
Blood Cells, Molecules & Diseases|February 6, 2008
Segmental duplications involving the alpha-globin gene cluster are causing beta-thalassemia intermedia phenotypes in beta-thalassemia heterozygous patientsC L Harteveld, C Refaldi, E Cassinerio, et al.
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.
Pageof 5