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R Ducrocq

Showing results (31-40 of 59) with videos related to

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Human Genetics|August 1, 1997
Polymorphism in exon 10 of the human coagulation factor V gene in a population at risk for sickle cell diseaseD Helley, C Besmond, R Ducrocq, et al.
Journal of Medical Screening|May 12, 1998
Compound heterozygosity Hb S/Hb Hope (beta 136 Gly-->Asp): a pitfall in the newborn screening for sickle cell diseaseR Ducrocq, A Bévier, A Leneveu, et al.
Fetal Diagnosis and Therapy|September 1, 1993
Measurement of adult hemoglobin in fetal blood samples by high-performance liquid chromatography as purity control for the prenatal diagnosis of chromosomal abnormalitiesR Ducrocq, G Tachdjian, J F Oury, et al.
American Journal of Hematology|July 1, 1994
Hemoglobinopathies in the Dogon Country: presence of beta S, beta C, and delta A' genesR Ducrocq, M Bennani, G Bellis, et al.
British Journal of Haematology|October 16, 1999
Purification, amplification and characterization of a population of human erythroid progenitorsJ M Freyssinier, C Lecoq-Lafon, S Amsellem, et al.
Blood|October 15, 1993
Beta-globin gene cluster haplotype and alpha-thalassemia do not correlate with the acute clinical manifestations of sickle cell disease in childrenM de Montalembert, M Maier-Redelsperger, R Girot, et al.
Blood|July 1, 1995
Bicentric origin of sickle hemoglobin among the inhabitants of Mauritius IslandN Kotea, S Baligadoo, S Surran, et al.
Hemoglobin|May 1, 1995
Two fetal hemoglobin variants affecting the same residue: Hb F-Emirates [G gamma 59(E3)Lys-->Glu] and Hb F-Sacromonte [G gamma 59(E3)Lys-->Gln]S Abbes, P A Fitzgerald, E Varady, et al.
Hemoglobin|March 18, 2000
Two new Ggamma chain variants: Hb F-clamart [gamma17(A14)Lys-->Asn] and Hb F-Ouled Rabah [gamma19(B1)Asn-->Lys]H Wajcman, K Borensztajn, J Riou, 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.
Pageof 6

Showing results (31-40 of 59) with videos related to

Sort By:
Pageof 6
Human Genetics|August 1, 1997
Polymorphism in exon 10 of the human coagulation factor V gene in a population at risk for sickle cell diseaseD Helley, C Besmond, R Ducrocq, et al.
Journal of Medical Screening|May 12, 1998
Compound heterozygosity Hb S/Hb Hope (beta 136 Gly-->Asp): a pitfall in the newborn screening for sickle cell diseaseR Ducrocq, A Bévier, A Leneveu, et al.
Fetal Diagnosis and Therapy|September 1, 1993
Measurement of adult hemoglobin in fetal blood samples by high-performance liquid chromatography as purity control for the prenatal diagnosis of chromosomal abnormalitiesR Ducrocq, G Tachdjian, J F Oury, et al.
American Journal of Hematology|July 1, 1994
Hemoglobinopathies in the Dogon Country: presence of beta S, beta C, and delta A' genesR Ducrocq, M Bennani, G Bellis, et al.
British Journal of Haematology|October 16, 1999
Purification, amplification and characterization of a population of human erythroid progenitorsJ M Freyssinier, C Lecoq-Lafon, S Amsellem, et al.
Blood|October 15, 1993
Beta-globin gene cluster haplotype and alpha-thalassemia do not correlate with the acute clinical manifestations of sickle cell disease in childrenM de Montalembert, M Maier-Redelsperger, R Girot, et al.
Blood|July 1, 1995
Bicentric origin of sickle hemoglobin among the inhabitants of Mauritius IslandN Kotea, S Baligadoo, S Surran, et al.
Hemoglobin|May 1, 1995
Two fetal hemoglobin variants affecting the same residue: Hb F-Emirates [G gamma 59(E3)Lys-->Glu] and Hb F-Sacromonte [G gamma 59(E3)Lys-->Gln]S Abbes, P A Fitzgerald, E Varady, et al.
Hemoglobin|March 18, 2000
Two new Ggamma chain variants: Hb F-clamart [gamma17(A14)Lys-->Asn] and Hb F-Ouled Rabah [gamma19(B1)Asn-->Lys]H Wajcman, K Borensztajn, J Riou, 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.
Pageof 6