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D Labie

Showing results (91-100 of 212) with videos related to

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FEBS Letters|January 15, 1976
Hb J Mexico in Algeria: arguments for an heterogenous distribution of alpha genesG Trabuchet, M Dahmane, J Pagnier, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1979
[Non-enzymatic hemoglobin glycosylation in the normal and diabetic patient]D Labie, H Wajcman, R Krishnamoorthy, et al.
Human Genetics|February 1, 1988
Analysis of crossover type in the alpha -3.7 haplotype among sickle cell anemia patients from various parts of AfricaC Dodé, A Berth, J Rochette, et al.
FEBS Letters|March 5, 1971
Consequences of heme loss in unstable hemoglobins: A study of hemoglobin kölnH Wajcman, V B&ycaron;cková, S Haidas, et al.
Acta Haematologica|January 1, 1976
A 2d case of haemoglobin Belfast (beta 15 (A 12) Trp replaced by Arg) observed in a French patientG Gacon, H Wajcman, D Labie, et al.
Annales De Medecine Interne|June 1, 1970
[Genetic control of hemoglobin biosynthesis and its abnormalities]G Schapira, J Kruh, D Labie, et al.
FEBS Letters|October 15, 1976
Structural and functional studies of haemoglobin Suresnes or alpha2 141 (HC3) Arg replaced by His beta2, a new high oxygen affinity mutantC Poyart, R Krishnamoorthy, E Bursaux, et al.
Haematologia|January 1, 1986
Heterogeneity of sickle cell disease as shown by density profiles: effects of fetal hemoglobin and alpha thalassemiaV Baudin, J Pagnier, D Labie, et al.
Hemoglobin|January 1, 1982
Hb J Daloa (beta 57 (E1) Asn replaced by Asp): a new variant found in Ivory CoastJ P Boissel, H Wajcman, D Labie, et al.
Human Biology|February 1, 1992
Rapid and direct detection of the most frequent Mediterranean beta-thalassemic mutations by multiplex allele-specific enzymatic amplificationT Bienvenu, P Sebillon, D Labie, et al.
Pageof 22

Showing results (91-100 of 212) with videos related to

Sort By:
Pageof 22
FEBS Letters|January 15, 1976
Hb J Mexico in Algeria: arguments for an heterogenous distribution of alpha genesG Trabuchet, M Dahmane, J Pagnier, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1979
[Non-enzymatic hemoglobin glycosylation in the normal and diabetic patient]D Labie, H Wajcman, R Krishnamoorthy, et al.
Human Genetics|February 1, 1988
Analysis of crossover type in the alpha -3.7 haplotype among sickle cell anemia patients from various parts of AfricaC Dodé, A Berth, J Rochette, et al.
FEBS Letters|March 5, 1971
Consequences of heme loss in unstable hemoglobins: A study of hemoglobin kölnH Wajcman, V B&ycaron;cková, S Haidas, et al.
Acta Haematologica|January 1, 1976
A 2d case of haemoglobin Belfast (beta 15 (A 12) Trp replaced by Arg) observed in a French patientG Gacon, H Wajcman, D Labie, et al.
Annales De Medecine Interne|June 1, 1970
[Genetic control of hemoglobin biosynthesis and its abnormalities]G Schapira, J Kruh, D Labie, et al.
FEBS Letters|October 15, 1976
Structural and functional studies of haemoglobin Suresnes or alpha2 141 (HC3) Arg replaced by His beta2, a new high oxygen affinity mutantC Poyart, R Krishnamoorthy, E Bursaux, et al.
Haematologia|January 1, 1986
Heterogeneity of sickle cell disease as shown by density profiles: effects of fetal hemoglobin and alpha thalassemiaV Baudin, J Pagnier, D Labie, et al.
Hemoglobin|January 1, 1982
Hb J Daloa (beta 57 (E1) Asn replaced by Asp): a new variant found in Ivory CoastJ P Boissel, H Wajcman, D Labie, et al.
Human Biology|February 1, 1992
Rapid and direct detection of the most frequent Mediterranean beta-thalassemic mutations by multiplex allele-specific enzymatic amplificationT Bienvenu, P Sebillon, D Labie, et al.
Pageof 22