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P C Giordano

Showing results (31-40 of 72) with videos related to

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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.
British Journal of Haematology|March 21, 2007
A new deletion defect leading to alpha-thalassaemia in a large Dutch Caucasian familyJ E Nooitgedagt, C L Harteveld, J S Starreveld, et al.
International Journal of Laboratory Hematology|August 4, 2010
Occurrence of common and rare δ-globin gene defects in two multiethnic populations: thirteen new mutations and the significance of δ-globin gene defects in β-thalassemia diagnosticsM Phylipsen, M V E Gallivan, S G J Arkesteijn, et al.
Nederlands Tijdschrift Voor Geneeskunde|June 17, 1989
[Combined alpha and beta thalassemia in a Chinese family in The Netherlands]M Losekoot, C Beijer, P C Giordano, et al.
International Journal of Laboratory Hematology|April 13, 2012
Hb Haaglanden: a new nonsickling β7Glu>Val variant. Consequences for basic diagnostics, screening, and risk assessment when dealing with HbS-like variantsC L Harteveld, G Ponjee, M Bakker-Verweij, et al.
European Journal of Medical Genetics|October 1, 2014
Sickle cell anemia and α-thalassemia: a modulating factor in homozygous HbS/S patients in OmanS M Hassan, M Al Muslahi, M Al Riyami, et al.
Prenatal Diagnosis|October 10, 2009
Prevention strategies for severe hemoglobinopathies in endemic and nonendemic immigration countries: the Latium exampleA Amato, P Grisanti, M Lerone, et al.
Human Genetics|September 1, 1997
alpha-Thalassemia in The Netherlands: a heterogeneous spectrum of both deletions and point mutationsK L Harteveld, M Losekoot, A J Heister, et al.
Hemoglobin|February 1, 1996
HB Gouda [alpha 72(EF1)His-->Gln], a new silent alpha chain variantP C Giordano, C L Harteveld, P J Kok, et al.
British Journal of Obstetrics and Gynaecology|July 1, 1997
The disappearance of fetal and donor red blood cells in alloimmunised pregnancies: a reappraisalJ Egberts, I L van Kamp, H H Kanhai, et al.
Pageof 8

Showing results (31-40 of 72) with videos related to

Sort By:
Pageof 8
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.
British Journal of Haematology|March 21, 2007
A new deletion defect leading to alpha-thalassaemia in a large Dutch Caucasian familyJ E Nooitgedagt, C L Harteveld, J S Starreveld, et al.
International Journal of Laboratory Hematology|August 4, 2010
Occurrence of common and rare δ-globin gene defects in two multiethnic populations: thirteen new mutations and the significance of δ-globin gene defects in β-thalassemia diagnosticsM Phylipsen, M V E Gallivan, S G J Arkesteijn, et al.
Nederlands Tijdschrift Voor Geneeskunde|June 17, 1989
[Combined alpha and beta thalassemia in a Chinese family in The Netherlands]M Losekoot, C Beijer, P C Giordano, et al.
International Journal of Laboratory Hematology|April 13, 2012
Hb Haaglanden: a new nonsickling β7Glu>Val variant. Consequences for basic diagnostics, screening, and risk assessment when dealing with HbS-like variantsC L Harteveld, G Ponjee, M Bakker-Verweij, et al.
European Journal of Medical Genetics|October 1, 2014
Sickle cell anemia and α-thalassemia: a modulating factor in homozygous HbS/S patients in OmanS M Hassan, M Al Muslahi, M Al Riyami, et al.
Prenatal Diagnosis|October 10, 2009
Prevention strategies for severe hemoglobinopathies in endemic and nonendemic immigration countries: the Latium exampleA Amato, P Grisanti, M Lerone, et al.
Human Genetics|September 1, 1997
alpha-Thalassemia in The Netherlands: a heterogeneous spectrum of both deletions and point mutationsK L Harteveld, M Losekoot, A J Heister, et al.
Hemoglobin|February 1, 1996
HB Gouda [alpha 72(EF1)His-->Gln], a new silent alpha chain variantP C Giordano, C L Harteveld, P J Kok, et al.
British Journal of Obstetrics and Gynaecology|July 1, 1997
The disappearance of fetal and donor red blood cells in alloimmunised pregnancies: a reappraisalJ Egberts, I L van Kamp, H H Kanhai, et al.
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