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Journal of Medical Genetics
|
September 1, 1975
A new case of haemoglobin Bucuresti in a Cuban family: further functional studies
B Colombe, M P Benitez, L Bernini, et al.
The Journal of Biological Chemistry
|
May 10, 1984
Covalent structures of beta and gamma autolytic derivatives of human alpha-thrombin
J P Boissel, B Le Bonniec, M J Rabiet, et al.
Hemoglobin
|
January 1, 1983
Silent beta-thalassemia associated with Hb Knossos beta 27 (B9) Ala replaced by Ser in Algeria
F Rouabhi, P Chardin, J P Boissel, et al.
Nouvelle Revue Francaise D'Hematologie
|
January 1, 1981
[Polymorphism of hemoglobins D in Ivory Coast: Hb Korle Bu (beta 73 (E17) Asp leads to Asn), Hb Avicenna (beta 47 (CD6) Asp leads to Ala) and Hb Cocody (beta 21 (B3) Asp leads to Asn) (author's transl)]
J P Boissel, H Fabritius, P Richard, et al.
Human Genetics
|
June 16, 1999
Genetic variations in human fetal globin gene microsatellites and their functional relevance
C Lapoumeroulie, L Castiglia, C Ruberto, et al.
La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris
|
April 23, 1977
[Clinical and biological aspects of beta-thalassemia. Apropos of 176 cases]
M Belhani, M Dahmane, F Richard, et al.
Blood
|
August 1, 1977
An unusual case of leukemia with high fetal hemoglobin: demonstration of abnormal hemoglobin synthesis localized in a red cell clone
J Pagnier, M Lopez, C Mathiot, et al.
Nouvelle Revue Francaise D'Hematologie
|
November 25, 1978
[Hemoglobin Pyrgos beta 83 (EF 7) Gly leads to Asp in a Malian: structural identification and functional properties (author's transl)]
H Wajcman, G Gacon, C Tudury, et al.
Hemoglobin
|
September 8, 1998
A novel polymorphism 3' to the beta-globin gene
C Badens, T Merghoub, D Lena-Russo, et al.
Nouvelle Revue Francaise D'Hematologie
|
May 1, 1972
[Biochemical study of a case of erythroleukemia. Demonstration in an abnormal erythrocyte population of simultaneous anomalies of hemoglobin and glycolysis enzymes]
J Pagnier, D Labie, J C Kaplan, et al.
Page
of 22
Search research articles
Search
Showing results (141-150 of 212) with videos related to
Sort By:
Page
of 22
Journal of Medical Genetics
|
September 1, 1975
A new case of haemoglobin Bucuresti in a Cuban family: further functional studies
B Colombe, M P Benitez, L Bernini, et al.
The Journal of Biological Chemistry
|
May 10, 1984
Covalent structures of beta and gamma autolytic derivatives of human alpha-thrombin
J P Boissel, B Le Bonniec, M J Rabiet, et al.
Hemoglobin
|
January 1, 1983
Silent beta-thalassemia associated with Hb Knossos beta 27 (B9) Ala replaced by Ser in Algeria
F Rouabhi, P Chardin, J P Boissel, et al.
Nouvelle Revue Francaise D'Hematologie
|
January 1, 1981
[Polymorphism of hemoglobins D in Ivory Coast: Hb Korle Bu (beta 73 (E17) Asp leads to Asn), Hb Avicenna (beta 47 (CD6) Asp leads to Ala) and Hb Cocody (beta 21 (B3) Asp leads to Asn) (author's transl)]
J P Boissel, H Fabritius, P Richard, et al.
Human Genetics
|
June 16, 1999
Genetic variations in human fetal globin gene microsatellites and their functional relevance
C Lapoumeroulie, L Castiglia, C Ruberto, et al.
La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris
|
April 23, 1977
[Clinical and biological aspects of beta-thalassemia. Apropos of 176 cases]
M Belhani, M Dahmane, F Richard, et al.
Blood
|
August 1, 1977
An unusual case of leukemia with high fetal hemoglobin: demonstration of abnormal hemoglobin synthesis localized in a red cell clone
J Pagnier, M Lopez, C Mathiot, et al.
Nouvelle Revue Francaise D'Hematologie
|
November 25, 1978
[Hemoglobin Pyrgos beta 83 (EF 7) Gly leads to Asp in a Malian: structural identification and functional properties (author's transl)]
H Wajcman, G Gacon, C Tudury, et al.
Hemoglobin
|
September 8, 1998
A novel polymorphism 3' to the beta-globin gene
C Badens, T Merghoub, D Lena-Russo, et al.
Nouvelle Revue Francaise D'Hematologie
|
May 1, 1972
[Biochemical study of a case of erythroleukemia. Demonstration in an abnormal erythrocyte population of simultaneous anomalies of hemoglobin and glycolysis enzymes]
J Pagnier, D Labie, J C Kaplan, et al.
Page
of 22