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International Journal of Laboratory Hematology
|
October 7, 2011
ICSH recommendations for the measurement of haemoglobin A2
A D Stephens, M Angastiniotis, E Baysal, 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 phenotype
C L Harteveld, P C Giordano, M Losekoot, et al.
Blood Cells, Molecules & Diseases
|
June 2, 2014
Molecular diagnostics of the HBB gene in an Omani cohort using bench-top DNA Ion Torrent PGM technology
S M Hassan, R H A M Vossen, R Chessa, et al.
Blood
|
February 15, 1991
Interaction of two different disorders in the beta-globin gene cluster associated with an increased hemoglobin F production: a novel deletion type of (G) gamma + ((A) gamma delta beta)(0)-thalassemia and a delta(0)-hereditary persistence of fetal hemoglobin determinant
M Losekoot, R Fodde, E J Gerritsen, et al.
International Journal of Laboratory Hematology
|
September 15, 2011
ICSH recommendations for the measurement of haemoglobin F
A D Stephens, M Angastiniotis, E Baysal, et al.
Hemoglobin
|
November 1, 1996
A Dutch family with Hb Atlanta [beta 75(E19)Leu-->Pro]
V Aygün, R van Zwieten, C J Pronk-Admiraal, et al.
Scandinavian Journal of Clinical and Laboratory Investigation
|
March 17, 2007
Epidemiology of haemoglobin disorders in Europe: an overview
B Modell, M Darlison, H Birgens, et al.
Annals of Hematology
|
October 1, 1996
Hb Malmö [beta-97(FG-4)His-->Gln] leading to polycythemia in a Dutch family
P C Giordano, C L Harteveld, A Brand, 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 mutation
P C Giordano, C L Harteveld, H L Haak, et al.
European Journal of Haematology
|
October 31, 2002
Hemoglobin H disease resulting from the association of the - alpha 3.7 rightward deletion and the (alpha alpha)MM deletion in a Brazilian patient
M R S C Wenning, C L Harteveld, P C Giordano, et al.
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of 8
Search research articles
Search
Showing results (51-60 of 72) with videos related to
Sort By:
Page
of 8
International Journal of Laboratory Hematology
|
October 7, 2011
ICSH recommendations for the measurement of haemoglobin A2
A D Stephens, M Angastiniotis, E Baysal, 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 phenotype
C L Harteveld, P C Giordano, M Losekoot, et al.
Blood Cells, Molecules & Diseases
|
June 2, 2014
Molecular diagnostics of the HBB gene in an Omani cohort using bench-top DNA Ion Torrent PGM technology
S M Hassan, R H A M Vossen, R Chessa, et al.
Blood
|
February 15, 1991
Interaction of two different disorders in the beta-globin gene cluster associated with an increased hemoglobin F production: a novel deletion type of (G) gamma + ((A) gamma delta beta)(0)-thalassemia and a delta(0)-hereditary persistence of fetal hemoglobin determinant
M Losekoot, R Fodde, E J Gerritsen, et al.
International Journal of Laboratory Hematology
|
September 15, 2011
ICSH recommendations for the measurement of haemoglobin F
A D Stephens, M Angastiniotis, E Baysal, et al.
Hemoglobin
|
November 1, 1996
A Dutch family with Hb Atlanta [beta 75(E19)Leu-->Pro]
V Aygün, R van Zwieten, C J Pronk-Admiraal, et al.
Scandinavian Journal of Clinical and Laboratory Investigation
|
March 17, 2007
Epidemiology of haemoglobin disorders in Europe: an overview
B Modell, M Darlison, H Birgens, et al.
Annals of Hematology
|
October 1, 1996
Hb Malmö [beta-97(FG-4)His-->Gln] leading to polycythemia in a Dutch family
P C Giordano, C L Harteveld, A Brand, 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 mutation
P C Giordano, C L Harteveld, H L Haak, et al.
European Journal of Haematology
|
October 31, 2002
Hemoglobin H disease resulting from the association of the - alpha 3.7 rightward deletion and the (alpha alpha)MM deletion in a Brazilian patient
M R S C Wenning, C L Harteveld, P C Giordano, et al.
Page
of 8