(Q39460685)

English

First description in Tunisia of a point mutation at codon 119 (CCT-->TCT) in the alpha1-globin gene: Hb Groene Hart in association with the -alpha3.7 deletion

scientific article published on January 2005

In more languages

default for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

12 September 2017

First description in Tunisia of a point mutation at codon 119 (CCT-->TCT) in the alpha1-globin gene: Hb Groene Hart in association with the -alpha3.7 deletion (English)

1 reference

Europe PubMed Central

PubMed publication ID

12 September 2017

1 reference

based on heuristic

inferred from title

author name string

Hajer Siala

1

1 reference

Europe PubMed Central

PubMed publication ID

12 September 2017

Faida Ouali

2

1 reference

Europe PubMed Central

PubMed publication ID

12 September 2017

Taieb Messaoud

3

1 reference

Europe PubMed Central

PubMed publication ID

12 September 2017

Rachida Sfar

4

1 reference

Europe PubMed Central

PubMed publication ID

12 September 2017

Slaheddine Fattoum

5

1 reference

Europe PubMed Central

PubMed publication ID

12 September 2017

publication date

1 January 2005

1 reference

Europe PubMed Central

PubMed publication ID

12 September 2017

1 reference

Europe PubMed Central

PubMed publication ID

12 September 2017

29

1 reference

Europe PubMed Central

PubMed publication ID

12 September 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

12 September 2017

263-268

1 reference

Europe PubMed Central

PubMed publication ID

12 September 2017

Rapid detection of alpha-thalassaemia deletions and alpha-globin gene triplication by multiplex polymerase chain reactions.

1 reference

https://api.crossref.org/works/10.1080%2F03630260500308053

21 January 2018

A PCR-based strategy to detect the common severe determinants of alpha thalassaemia

1 reference

https://api.crossref.org/works/10.1080%2F03630260500308053

21 January 2018

A mismatched-primer polymerase chain reaction-restriction fragment length polymorphism strategy for rapid screening of the polyadenylation signal mutation alpha(T-Saudi) (AATAAA-->AATAAG) in the alpha2-globin gene

1 reference

https://api.crossref.org/works/10.1080%2F03630260500308053

21 January 2018

A novel alpha-thalassemia nonsense mutation in codon 23 of the alpha2-globin gene (GAG-->TAG) in a Tunisian family

1 reference

https://api.crossref.org/works/10.1080%2F03630260500308053

21 January 2018

Denaturing HPLC-based assay for molecular screening of nondeletional mutations causing alpha-thalassemias

1 reference

https://api.crossref.org/works/10.1080%2F03630260500308053

21 January 2018

Molecular spectrum of alpha-thalassemia in Tunisia: epidemiology and detection at birth

1 reference

https://api.crossref.org/works/10.1080%2F03630260500308053

21 January 2018

Identifiers

10.1080/03630260500308053

1 reference

Europe PubMed Central

PubMed publication ID

12 September 2017

release_c6rquqbulvhrjfpbwgk3cbkf4u

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

12 September 2017

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q39460685&oldid=1874743153"