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P Van Delft

Showing results (1-10 of 12) 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.
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.
International Journal of Laboratory Hematology|June 3, 2009
Evaluating five dedicated automatic devices for haemoglobinopathy diagnostics in multi-ethnic populationsP Van Delft, E Lenters, M Bakker-Verweij, 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.
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.
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.
Biochimie|September 4, 2025
Functional characterization of a plastidial cytochrome b5-fused Δ4-desaturase from Ostreococcus tauri in higher plantsM Miklaszewska, R E Gomez, P Van Delft, 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.
Hemoglobin|May 21, 1999
Hb Nijkerk: a new mutation at codons 138/139 of the beta-globin gene inducing severe hemolytic anemia in a Dutch girlH M van den Berg, M C Bruin, D Batelaan, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

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Pageof 2
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.
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.
International Journal of Laboratory Hematology|June 3, 2009
Evaluating five dedicated automatic devices for haemoglobinopathy diagnostics in multi-ethnic populationsP Van Delft, E Lenters, M Bakker-Verweij, 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.
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.
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.
Biochimie|September 4, 2025
Functional characterization of a plastidial cytochrome b5-fused Δ4-desaturase from Ostreococcus tauri in higher plantsM Miklaszewska, R E Gomez, P Van Delft, 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.
Hemoglobin|May 21, 1999
Hb Nijkerk: a new mutation at codons 138/139 of the beta-globin gene inducing severe hemolytic anemia in a Dutch girlH M van den Berg, M C Bruin, D Batelaan, et al.
Pageof 2