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Blood
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September 1, 1981
The sickle gene polymorphism in North Africa
J G Mears, C Beldjord, M Benabadji, et al.
American Journal of Hematology
|
April 1, 1993
Unstable alpha-chain hemoglobin variants with factitious beta-thalassemia biosynthetic ratio: Hb Questembert (alpha 131[H14]Ser-->Pro) and Hb Caen (alpha 132[H15]Val-->Gly)
H Wajcman, C Vasseur, Y Blouquit, et al.
Human Mutation
|
January 1, 1996
Novel and unusual deletion-insertion thalassemic mutation in exon 1 of the beta-globin gene
C Badens, I Thuret, G Michel, et al.
Human Genetics
|
March 1, 1997
Molecular basis of alpha-thalassemia in Sicily
M Fichera, A Spalletta, F Fiorenza, et al.
Nouvelle Revue Francaise D'Hematologie
|
January 1, 1979
[Hemoglobin J Amiens beta 17 (A 14) Lys replaced by Asn. Coincidence of a functionally silent new abnormal hemoglobin and a polycythemia vera (author's transl)]
J Elion, H Wajcman, O Belkhodja-Dunda, et al.
Blood
|
February 1, 1992
DNA sequence variation in a negative control region 5' to the beta-globin gene correlates with the phenotypic expression of the beta s mutation
J Elion, P E Berg, C Lapouméroulie, et al.
La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris
|
December 8, 1978
[Hemoglobinopathies in West-African immigrant workers in France (author's transl)]
D Labie, K P Amegnizin, H Wajcman, et al.
Blood
|
July 1, 1995
Bicentric origin of sickle hemoglobin among the inhabitants of Mauritius Island
N Kotea, S Baligadoo, S Surran, et al.
Nouvelle Revue Francaise D'Hematologie
|
January 1, 1982
Haemoglobin A2 is elevated in hyperthyroid patients
R Krishnamoorthy, J Elion, J M Kuhn, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 1, 1984
Evidence for the multicentric origin of the sickle cell hemoglobin gene in Africa
J Pagnier, J G Mears, O Dunda-Belkhodja, et al.
Page
of 22
Search research articles
Search
Showing results (181-190 of 212) with videos related to
Sort By:
Page
of 22
Blood
|
September 1, 1981
The sickle gene polymorphism in North Africa
J G Mears, C Beldjord, M Benabadji, et al.
American Journal of Hematology
|
April 1, 1993
Unstable alpha-chain hemoglobin variants with factitious beta-thalassemia biosynthetic ratio: Hb Questembert (alpha 131[H14]Ser-->Pro) and Hb Caen (alpha 132[H15]Val-->Gly)
H Wajcman, C Vasseur, Y Blouquit, et al.
Human Mutation
|
January 1, 1996
Novel and unusual deletion-insertion thalassemic mutation in exon 1 of the beta-globin gene
C Badens, I Thuret, G Michel, et al.
Human Genetics
|
March 1, 1997
Molecular basis of alpha-thalassemia in Sicily
M Fichera, A Spalletta, F Fiorenza, et al.
Nouvelle Revue Francaise D'Hematologie
|
January 1, 1979
[Hemoglobin J Amiens beta 17 (A 14) Lys replaced by Asn. Coincidence of a functionally silent new abnormal hemoglobin and a polycythemia vera (author's transl)]
J Elion, H Wajcman, O Belkhodja-Dunda, et al.
Blood
|
February 1, 1992
DNA sequence variation in a negative control region 5' to the beta-globin gene correlates with the phenotypic expression of the beta s mutation
J Elion, P E Berg, C Lapouméroulie, et al.
La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris
|
December 8, 1978
[Hemoglobinopathies in West-African immigrant workers in France (author's transl)]
D Labie, K P Amegnizin, H Wajcman, et al.
Blood
|
July 1, 1995
Bicentric origin of sickle hemoglobin among the inhabitants of Mauritius Island
N Kotea, S Baligadoo, S Surran, et al.
Nouvelle Revue Francaise D'Hematologie
|
January 1, 1982
Haemoglobin A2 is elevated in hyperthyroid patients
R Krishnamoorthy, J Elion, J M Kuhn, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 1, 1984
Evidence for the multicentric origin of the sickle cell hemoglobin gene in Africa
J Pagnier, J G Mears, O Dunda-Belkhodja, et al.
Page
of 22