(Q38943999)

7 September 2017

The peculiar spectrum of beta-thalassemia genes in Tunisia (English)

1 reference

7 September 2017

1 reference

1 reference

J Chibani

1

1 reference

7 September 2017

M Vidaud

2

1 reference

7 September 2017

P Duquesnoy

3

1 reference

7 September 2017

J L Bergé-Lefranc

4

1 reference

7 September 2017

M Pirastu

5

1 reference

7 September 2017

F Ellouze

6

1 reference

7 September 2017

J Rosa

7

1 reference

7 September 2017

M Goossens

8

1 reference

7 September 2017

1 February 1988

1 reference

7 September 2017

1 reference

7 September 2017

78

1 reference

7 September 2017

190-192

1 reference

7 September 2017

2

1 reference

https://scigraph.springernature.com/pub.10.1007/bf00278196

7 September 2017

0 references

cites work

The same beta-globin gene mutation is present on nine different beta-thalassemia chromosomes in a Sardinian population

1 reference

12 December 2020

Quantification of the close association between DNA haplotypes and specific β-thalassaemia mutations in Mediterraneans

1 reference

12 December 2020

Prenatal diagnosis of beta-thalassemia. Detection of a single nucleotide mutation in DNA

1 reference

12 December 2020

Polymorphism and molecular pathology of the human beta-globin gene

1 reference

12 December 2020

Heterogeneity of haplotypes among patients with severe Cooley disease in Eastern Sicily

1 reference

12 December 2020

Detection of sickle cell beta S-globin allele by hybridization with synthetic oligonucleotides

1 reference

12 December 2020

Linkage of beta-thalassaemia mutations and beta-globin gene polymorphisms with DNA polymorphisms in human beta-globin gene cluster.

1 reference

12 December 2020

Nonrandom association of polymorphic restriction sites in the β-globin gene cluster

1 reference

12 December 2020

Nonuniform recombination within the human beta-globin gene cluster

1 reference

12 December 2020

Spontaneous mutation in beta-thalassaemia producing the same nucleotide substitution as that in a common hereditary form

1 reference

12 December 2020

Beta A and beta thal DNA haplotypes in Sicily

1 reference

12 December 2020

Four new haplotypes observed in Algerian beta-thalassemia patients.

1 reference

12 December 2020

Specific transcription and RNA splicing defects in five cloned β-thalassaemia genes

1 reference

12 December 2020

DNA analysis in the diagnosis of hemoglobin disorders

1 reference

12 December 2020

A β-thalassemia ledon abolishes the sameMstII site as the sickle mutation

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00278196

1 reference

Dimensions Publication ID

7 September 2017

0 references

1 reference