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J Elion

Showing results (151-160 of 189) with videos related to

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Thrombosis and Haemostasis|November 1, 2000
Ethnic heterogeneity of the factor XIII Val34Leu polymorphismF A Attié-Castro, M A Zago, J Lavinha, et al.
Blood|June 17, 1998
Fetal hemoglobin and F-cell responses to long-term hydroxyurea treatment in young sickle cell patients. The French Study Group on Sickle Cell DiseaseM Maier-Redelsperger, M de Montalembert, A Flahault, et al.
Molecular Genetics and Metabolism|February 13, 2001
Molecular and structural analysis of two novel mutations in a patient with mut(-) methylmalonyl-CoA deficiencyJ F Benoist, C Acquaviva, I Callebaut, et al.
Annals of the New York Academy of Sciences|July 21, 1998
Molecular basis of beta-thalassemia in Bahrain: an epicenter for a Middle East specific mutationN Jassim, T Merghoub, O Pascaud, et al.
Transplantation|May 1, 1992
HLA-mismatched cord-blood transplantation in a patient with advanced leukemiaE Vilmer, G Sterkers, C Rahimy, et al.
Human Genetics|September 1, 1991
Nucleotide sequence evidence of the unicentric origin of the beta C mutation in AfricaG Trabuchet, J Elion, O Dunda, et al.
European Journal of Human Genetics : EJHG|February 5, 1998
Haemoglobin D-Ouled Rabah among the Mozabites: a relevant variant to trace the origin of Berber-speaking populationsT Merghoub, A Sanchez-Mazas, R Tamouza, et al.
Human Biology|June 1, 1994
Anthropological approach to the heterogeneity of beta-thalassemia mutations in northern AfricaC Bennani, R Bouhass, P Perrin-Pecontal, et al.
European Journal of Human Genetics : EJHG|August 31, 2001
N219Y, a new frequent mutation among mut(degree) forms of methylmalonic acidemia in Caucasian patientsC Acquaviva, J F Benoist, I Callebaut, et al.
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.
Pageof 19

Showing results (151-160 of 189) with videos related to

Sort By:
Pageof 19
Thrombosis and Haemostasis|November 1, 2000
Ethnic heterogeneity of the factor XIII Val34Leu polymorphismF A Attié-Castro, M A Zago, J Lavinha, et al.
Blood|June 17, 1998
Fetal hemoglobin and F-cell responses to long-term hydroxyurea treatment in young sickle cell patients. The French Study Group on Sickle Cell DiseaseM Maier-Redelsperger, M de Montalembert, A Flahault, et al.
Molecular Genetics and Metabolism|February 13, 2001
Molecular and structural analysis of two novel mutations in a patient with mut(-) methylmalonyl-CoA deficiencyJ F Benoist, C Acquaviva, I Callebaut, et al.
Annals of the New York Academy of Sciences|July 21, 1998
Molecular basis of beta-thalassemia in Bahrain: an epicenter for a Middle East specific mutationN Jassim, T Merghoub, O Pascaud, et al.
Transplantation|May 1, 1992
HLA-mismatched cord-blood transplantation in a patient with advanced leukemiaE Vilmer, G Sterkers, C Rahimy, et al.
Human Genetics|September 1, 1991
Nucleotide sequence evidence of the unicentric origin of the beta C mutation in AfricaG Trabuchet, J Elion, O Dunda, et al.
European Journal of Human Genetics : EJHG|February 5, 1998
Haemoglobin D-Ouled Rabah among the Mozabites: a relevant variant to trace the origin of Berber-speaking populationsT Merghoub, A Sanchez-Mazas, R Tamouza, et al.
Human Biology|June 1, 1994
Anthropological approach to the heterogeneity of beta-thalassemia mutations in northern AfricaC Bennani, R Bouhass, P Perrin-Pecontal, et al.
European Journal of Human Genetics : EJHG|August 31, 2001
N219Y, a new frequent mutation among mut(degree) forms of methylmalonic acidemia in Caucasian patientsC Acquaviva, J F Benoist, I Callebaut, et al.
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.
Pageof 19