(Q73531171)

English

The prothrombin nt20210 A allele as a risk factor for venous thromboembolism: detection of heterozygous and homozygous carriers by alternative methods

scientific article published on 01 March 2000

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scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10709912%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

The prothrombin nt20210 A allele as a risk factor for venous thromboembolism: detection of heterozygous and homozygous carriers by alternative methods (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10709912%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

venous thromboembolism

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

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author name string

M Meyer

1

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10709912%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

G Kutscher

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10709912%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

G Vogel

3

1 reference

Europe PubMed Central

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4 November 2019

publication date

1 March 2000

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4 November 2019

Thrombosis Research

1 reference

Europe PubMed Central

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4 November 2019

97

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4 November 2019

5

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4 November 2019

359-363

1 reference

Europe PubMed Central

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4 November 2019

Mutation in blood coagulation factor V associated with resistance to activated protein C.

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900177-2

7 January 2021

based on heuristic

inferred from DOI database lookup

The heterozygous 20210 G/A prothrombin genotype is associated with early venous thrombosis in inherited thrombophilias and is not increased in frequency in artery disease

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900177-2

7 January 2021

based on heuristic

inferred from DOI database lookup

A prothrombin gene mutation is significantly associated with venous thrombosis

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900177-2

7 January 2021

based on heuristic

inferred from DOI database lookup

The prothrombin gene G20210A variant: prevalence in a U.K. anticoagulant clinic population

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900177-2

7 January 2021

based on heuristic

inferred from DOI database lookup

A patient homozygous for a mutation in the prothrombin gene 3'-untranslated region associated with massive thrombosis

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900177-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900177-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900177-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in the catalytic domain of human coagulation factor IX: rapid characterization by direct genomic sequencing of DNA fragments displaying an altered melting behavior

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900177-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0049-3848(99)00177-2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10709912%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10709912%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

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