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P C Giordano

Showing results (21-30 of 72) with videos related to

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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.
Hemoglobin|January 1, 1990
Hb J-Anatolia [alpha 61(E10)Lys----Thr]: structural characterization and gene localization of a new alpha chain variantP C Giordano, R Fodde, R Amons, 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.
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.
Journal of Health and Social Behavior|May 12, 1998
The quality of adolescent friendships: long-term effects?P C Giordano, S A Cernkovich, H T Groat, 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.
International Journal of Laboratory Hematology|December 18, 2012
Basic haemoglobinopathy diagnostics in Dutch laboratories; providing an informative test resultJ O Kaufmann, J W Smit, W Huisman, 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.
American Journal of Hematology|September 26, 2003
Molecular spectrum of alpha-thalassemia in the Iranian population of Hormozgan: three novel point mutation defectsC L Harteveld, M Yavarian, A Zorai, 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.
Pageof 8

Showing results (21-30 of 72) with videos related to

Sort By:
Pageof 8
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.
Hemoglobin|January 1, 1990
Hb J-Anatolia [alpha 61(E10)Lys----Thr]: structural characterization and gene localization of a new alpha chain variantP C Giordano, R Fodde, R Amons, 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.
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.
Journal of Health and Social Behavior|May 12, 1998
The quality of adolescent friendships: long-term effects?P C Giordano, S A Cernkovich, H T Groat, 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.
International Journal of Laboratory Hematology|December 18, 2012
Basic haemoglobinopathy diagnostics in Dutch laboratories; providing an informative test resultJ O Kaufmann, J W Smit, W Huisman, 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.
American Journal of Hematology|September 26, 2003
Molecular spectrum of alpha-thalassemia in the Iranian population of Hormozgan: three novel point mutation defectsC L Harteveld, M Yavarian, A Zorai, 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.
Pageof 8