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D Labie

Showing results (201-210 of 212) with videos related to

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Nouvelle Revue Francaise D'Hematologie|October 1, 1994
Fetal haemoglobin variations following hydroxyurea treatment in patients with cyanotic congenital heart diseaseP Triadou, M Maier-Redelsperger, R Krishnamoorty, et al.
Human Genetics|May 1, 1992
A novel sickle cell mutation of yet another origin in Africa: the Cameroon typeC Lapouméroulie, O Dunda, R Ducrocq, et al.
Sangre|January 1, 1981
[Haemoglobin Fannin-Lubbock (alpha 2 beta 2 119 (GH2) Gly leads to Asp). Report of the first case found in Europe)]J L Aguilar i Bascompte, H Wajcman, J L Vives i Corrons, et al.
American Journal of Hematology|April 1, 1995
Abnormal hemoglobins in Mauritius IslandN Kotea, R DuCrocq, S K Surrun, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1985
Common haplotype dependency of high G gamma-globin gene expression and high Hb F levels in beta-thalassemia and sickle cell anemia patientsD Labie, J Pagnier, C Lapoumeroulie, et al.
Human Biology|December 1, 1992
Importation route of the sickle cell trait into Portugal: contribution of molecular epidemiologyJ Lavinha, J Gonçalves, P Faustino, et al.
Blood|March 15, 1996
Variation of fetal hemoglobin and F-cell number with the LCR-HS2 polymorphism in nonanemic individualsT Merghoub, M Maier-Redelsperger, D Labie, et al.
Nature|February 28, 1980
Beta-chain contact sites in the haemoglobin S polymerR L Nagel, J Johnson, R M Bookchin, et al.
American Journal of Hematology|December 12, 1997
Dissection of the association status of two polymorphisms in the beta-globin gene cluster with variations in F-cell number in non-anemic individualsT Merghoub, B Perichon, M Maier-Redelsperger, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1979
Structural bases of the inhibitory effects of hemoglobin F and hemoglobin A2 on the polymerization of hemoglobin SR L Nagel, R M Bookchin, J Johnson, et al.
Pageof 22

Showing results (201-210 of 212) with videos related to

Sort By:
Pageof 22
Nouvelle Revue Francaise D'Hematologie|October 1, 1994
Fetal haemoglobin variations following hydroxyurea treatment in patients with cyanotic congenital heart diseaseP Triadou, M Maier-Redelsperger, R Krishnamoorty, et al.
Human Genetics|May 1, 1992
A novel sickle cell mutation of yet another origin in Africa: the Cameroon typeC Lapouméroulie, O Dunda, R Ducrocq, et al.
Sangre|January 1, 1981
[Haemoglobin Fannin-Lubbock (alpha 2 beta 2 119 (GH2) Gly leads to Asp). Report of the first case found in Europe)]J L Aguilar i Bascompte, H Wajcman, J L Vives i Corrons, et al.
American Journal of Hematology|April 1, 1995
Abnormal hemoglobins in Mauritius IslandN Kotea, R DuCrocq, S K Surrun, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1985
Common haplotype dependency of high G gamma-globin gene expression and high Hb F levels in beta-thalassemia and sickle cell anemia patientsD Labie, J Pagnier, C Lapoumeroulie, et al.
Human Biology|December 1, 1992
Importation route of the sickle cell trait into Portugal: contribution of molecular epidemiologyJ Lavinha, J Gonçalves, P Faustino, et al.
Blood|March 15, 1996
Variation of fetal hemoglobin and F-cell number with the LCR-HS2 polymorphism in nonanemic individualsT Merghoub, M Maier-Redelsperger, D Labie, et al.
Nature|February 28, 1980
Beta-chain contact sites in the haemoglobin S polymerR L Nagel, J Johnson, R M Bookchin, et al.
American Journal of Hematology|December 12, 1997
Dissection of the association status of two polymorphisms in the beta-globin gene cluster with variations in F-cell number in non-anemic individualsT Merghoub, B Perichon, M Maier-Redelsperger, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1979
Structural bases of the inhibitory effects of hemoglobin F and hemoglobin A2 on the polymerization of hemoglobin SR L Nagel, R M Bookchin, J Johnson, et al.
Pageof 22