The peculiar spectrum of β-thalassemia genes in Tunisia

Human Genetics

Volumn 78, Issue 2, 1988, Pages 190-192

  Chibani, J ^a   Vidaud, M ^b,c   Duquesnoy, P ^b,c   Berge Lefranc J L ^b   Pirastu, M ^d   Ellouze, F ^a   Rosa, J ^b,c   Goossens, M ^b,c  

^a UNIVERSITY OF MONASTIR   (Tunisia)

^b INSERM   (France)

^c HENRI MONDOR HOSPITAL   (France)

^d CNR   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

BETA GLOBIN; OLIGONUCLEOTIDE;

BETA THALASSEMIA; CLINICAL ARTICLE; GENE CLUSTER; GENETIC ENGINEERING; HEREDITY; HUMAN; HUMAN CELL; MUTATION; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; TUNISIA;

GENETIC MARKERS; GLOBINS; HUMAN; MUTATION; SUPPORT, NON-U.S. GOV'T; THALASSEMIA; TUNISIA;

EID: 0023849720     PISSN: 03406717     EISSN: 14321203     Source Type: Journal    
DOI: 10.1007/BF00278196     Document Type: Article

References (17)

1. Nonrandom association of polymorphic restriction sites in the β-globin gene cluster
2. Four new haplotypes observed in Algerian β-thalassemia patients
3. Non-uniform recombination within the β-globin gene cluster
4. A β-thalassemia lesion abolishes the same Mst II site as the sickle mutation
5. Spontaneous mutation in β-thalassaemia producing the same nucleotide substitution as that in a common hereditary form
6. s-globin allele by hybridization with synthetic oligonucleotides
7. DNA analysis in the diagnosis of hemoglobin disorders
8. Quantification of the close association between DNA haplotypes and specific β-thalassemia mutations in Mediterraneans
9. Heterogeneity of haplotypes among patients with severe Cooley disease in Eastern Sicily
10. Linkage of β thalassemia mutations and β globin gene polymorphisms with DNA polymorphisms in human β globin gene cluster
11. Polymorphism and molecular pathology of the human β-globin gene
12. Prenatal diagnosis of β-thalassemia: detection of a single nucleotide mutation in DNA
13. The same β-globin gene mutation is present on nine different β-thalassemia chromosomes in a Sardinian population
14. Specific transcription and RNA splicing defects in five cloned β-thalassemia genes