Literature DB >> 3667319

Oligonucleotide screening of beta thalassemia mutations in the south east of France.

M Milland1, J L Bergé-Lefranc, D Lena, G Cartouzou.   

Abstract

France is a non-endemic region for beta thalassemia. In this country, the sporadic cases of Cooley's disease encountered affect almost constantly subjects of Mediterranean origin. In this report, we have screened, using oligonucleotide probes, the distribution of the main beta thalassemia mutations present in the population of South-eastern France whose origins lie in the mixing of several Mediterranean ethnic groups. Among 105 beta thalassemia chromosomes, we have observed a limited number of alleles, since, by using oligonucleotide probes for six mutations, we have characterized the molecular defect in 90% of the chromosomes. The four main mutations were found in more than 85% of the chromosomes and the others in about 5%. The distribution of the beta thalassemia mutations within the various ethnic groups was determined.

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Year:  1987        PMID: 3667319     DOI: 10.3109/03630268709042851

Source DB:  PubMed          Journal:  Hemoglobin        ISSN: 0363-0269            Impact factor:   0.849


  3 in total

1.  The molecular basis of beta-thalassemia in Turkey.

Authors:  A N Başak; H Ozçelik; A Ozer; A Tolun; M Aksoy; L Ağaoğlu; F Ridolfi; L Ulukutlu; N Akar; A Gürgey
Journal:  Hum Genet       Date:  1992-05       Impact factor: 4.132

2.  Prenatal diagnosis of beta thalassaemia by oligonucleotide analysis in Mediterranean populations.

Authors:  M C Rosatelli; T Tuveri; M T Scalas; A Di Tucci; G B Leoni; M Furbetta; G Monni; A Cao
Journal:  J Med Genet       Date:  1988-11       Impact factor: 6.318

3.  Beta thalassaemia mutations in Turkish Cypriots.

Authors:  A Sozuoz; A Berkalp; A Figus; A Loi; M Pirastu; A Cao
Journal:  J Med Genet       Date:  1988-11       Impact factor: 6.318

  3 in total

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