R Benarous|D Labie|F Josso - JoVE Visualize

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Biochemical and Biophysical Research Communications|September 14, 1986

Beta thalassemia due to a novel mutation in IVS 1 sequence donor site consensus sequence creating a restriction siteC Lapoumeroulie, J Pagnier, A Bank, 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.

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.

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.

Thrombosis Research|September 15, 1982

Fibrinogen Bondy: a new case of dysfibrinogenemia. Isolation of the abnormal fibrinogen moleculesM Jandrot-Perrus, M H Aurousseau, M J Rabiet, et al.

Leukemia|February 1, 1993

Selective increase of alternatively spliced Lck transcripts from the proximal promotor in hematopoietic malignanciesE Rouer, F Dreyfus, J Melle, et al.

Proceedings of the National Academy of Sciences of the United States of America|August 1, 1986

Cloning and expression of cDNA for anti-müllerian hormoneJ Y Picard, R Benarous, D Guerrier, et al.

Histochemistry|January 1, 1990

Tissue-plasminogen activator RNA detected in megakaryocytes by in situ hybridization and biotinylated probeC Brisson-Jeanneau, L Nelles, E Rouer, 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 21

Showing results (61-70 of 208) with videos related to

Sort By:

Pageof 21

Biochemical and Biophysical Research Communications|September 14, 1986

Beta thalassemia due to a novel mutation in IVS 1 sequence donor site consensus sequence creating a restriction siteC Lapoumeroulie, J Pagnier, A Bank, 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.

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.

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.

Thrombosis Research|September 15, 1982

Fibrinogen Bondy: a new case of dysfibrinogenemia. Isolation of the abnormal fibrinogen moleculesM Jandrot-Perrus, M H Aurousseau, M J Rabiet, et al.

Leukemia|February 1, 1993

Selective increase of alternatively spliced Lck transcripts from the proximal promotor in hematopoietic malignanciesE Rouer, F Dreyfus, J Melle, et al.

Proceedings of the National Academy of Sciences of the United States of America|August 1, 1986

Cloning and expression of cDNA for anti-müllerian hormoneJ Y Picard, R Benarous, D Guerrier, et al.

Histochemistry|January 1, 1990

Tissue-plasminogen activator RNA detected in megakaryocytes by in situ hybridization and biotinylated probeC Brisson-Jeanneau, L Nelles, E Rouer, 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 21