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G Lefranc

Biographic Data

ID3910744
NAMEG Lefranc
GIVEN NAMESG
FAMILY NAMELefranc
SIGNATURELEFRANC G
VERIFIEDNo
TOTAL WORKS3
TOTAL CITATIONS1
AUTHOR COUNT3
EDITOR COUNT0
FIRST PUBLICATION YEAR1976
LATEST PUBLICATION YEAR2012
H-INDEX1
  • Synthetic review on the different anthropological aspects of hemoglobinopathies in Tunisia

    Open Access•AH Khelil, P Perrin et al.•ARTICLE•International Journal of Modern…•2012

    Hemoglobinopathies are a group of hereditary hemolytic anemia characterized by qualitative (sickle cell disease) or quantitative (thalassemia) defects in the alpha or beta-globin chain synthesis. Homozygotes or compound heterozygotes for the mutated alpha or beta-globin genes can cause severe anemia at an early age. These pathologies are common in some areas (Mediterranean, Africa, India, and Southeast Asia). Tunisia, by its geographical location…

  • A Worldwide Analysis of AG Molecular Diversity Inferred from Serology

    Alicia Sanchez‐maza, A Sanchez-Mazas et al.•ARTICLE•Human Biology•2001•Cited by: 1•References: 3

    Ten population samples from different geographic origins were tested serologically for the AG polymorphism of human beta-lipoproteins. Their haplotype frequencies were used with previously published data to perform a wide analysis of AG genetic differentiations throughout the world. Coancestry coefficients were computed from weighted F(ST)s among populations by using a matrix of molecular distances among AG haplotypes, which is here determined on…

  • L'aloi des monnaies d'or à Cambrai de 1347 à 1974

    G Lefranc•ARTICLE•Revue du Nord•1976

    G. LEFRANC, Fineness of gold coinage in Cambrai between 1347 and 1974. The Cambray County in the person of its bishop, was recognized in 742 by Pépin le Bref as quasi-independant. The first Germanic Roman Emperors , having become its Suzerains, confirmed it. In 1347, the bishop Guy IV de Ventadour minted the first gold coin : the gold "Maille" or Florin. Until the Spanish domination at the end of the XVIth century, followed in 1677 by its incorpo…

  • A Worldwide Analysis of AG Molecular Diversity Inferred from Serology

    Alicia Sanchez‐maza, A Sanchez-Mazas et al.•ARTICLE•Human Biology•2001•Cited by: 1•References: 3

    Ten population samples from different geographic origins were tested serologically for the AG polymorphism of human beta-lipoproteins. Their haplotype frequencies were used with previously published data to perform a wide analysis of AG genetic differentiations throughout the world. Coancestry coefficients were computed from weighted F(ST)s among populations by using a matrix of molecular distances among AG haplotypes, which is here determined on…

  • L'aloi des monnaies d'or à Cambrai de 1347 à 1974

    G Lefranc•ARTICLE•Revue du Nord•1976

    G. LEFRANC, Fineness of gold coinage in Cambrai between 1347 and 1974. The Cambray County in the person of its bishop, was recognized in 742 by Pépin le Bref as quasi-independant. The first Germanic Roman Emperors , having become its Suzerains, confirmed it. In 1347, the bishop Guy IV de Ventadour minted the first gold coin : the gold "Maille" or Florin. Until the Spanish domination at the end of the XVIth century, followed in 1677 by its incorpo…

  • A Worldwide Analysis of AG Molecular Diversity Inferred from Serology

    Alicia Sanchez‐maza, A Sanchez-Mazas et al.•ARTICLE•Human Biology•2001•Cited by: 1•References: 3

    Ten population samples from different geographic origins were tested serologically for the AG polymorphism of human beta-lipoproteins. Their haplotype frequencies were used with previously published data to perform a wide analysis of AG genetic differentiations throughout the world. Coancestry coefficients were computed from weighted F(ST)s among populations by using a matrix of molecular distances among AG haplotypes, which is here determined on…

  • Synthetic review on the different anthropological aspects of hemoglobinopathies in Tunisia

    Open Access•AH Khelil, P Perrin et al.•ARTICLE•International Journal of Modern…•2012

    Hemoglobinopathies are a group of hereditary hemolytic anemia characterized by qualitative (sickle cell disease) or quantitative (thalassemia) defects in the alpha or beta-globin chain synthesis. Homozygotes or compound heterozygotes for the mutated alpha or beta-globin genes can cause severe anemia at an early age. These pathologies are common in some areas (Mediterranean, Africa, India, and Southeast Asia). Tunisia, by its geographical location…

Allele (2 works) · Biology (2 works) · Gene (2 works) · Genetics (2 works) · Genetics (2 works) · Haplotype (2 works) · Art (1 works) · Beta thalassemia (1 works) · Consanguinity (1 works) · Demography (1 works)

Ethnos_APP • Open Source Project • MIT License • Frontend v2.0.0 • Privacy and Cookies • API Documentation: api.ethnos.app/docs • API Source Code: GitHub • DOI: 10.5281/zenodo.17049435 • Frontend Source Code: GitHub • DOI: 10.5281/zenodo.17050053 • cruz.rio.br • Expectantes Misericordiae