Marie‐paule Lefranc
Biographic Data
| ID | 4787657 |
|---|---|
| NAME | Marie‐paule Lefranc |
| GIVEN NAMES | Marie‐paule |
| FAMILY NAME | Lefranc |
| SIGNATURE | LEFRANC M P |
| AFFILIATIONS | University of Monastir |
| ORCID | 0000-0003-0116-9353 |
| VERIFIED | Yes |
| TOTAL WORKS | 2 |
| TOTAL CITATIONS | 1 |
| AUTHOR COUNT | 2 |
| EDITOR COUNT | 0 |
| FIRST PUBLICATION YEAR | 2001 |
| LATEST PUBLICATION YEAR | 2012 |
| H-INDEX | 1 |
Synthetic review on the different anthropological aspects of hemoglobinopathies in Tunisia
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
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…
A Worldwide Analysis of AG Molecular Diversity Inferred from Serology
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…
A Worldwide Analysis of AG Molecular Diversity Inferred from Serology
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
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) · Beta thalassemia (1 works) · Consanguinity (1 works) · Demography (1 works) · Demography (1 works)