(Q31912670)

5 July 2017

title

Mutations in the ALK-1 gene and the phenotype of hereditary hemorrhagic telangiectasia in two large Danish families (English)

1 reference

hereditary hemorrhagic telangiectasia

5 July 2017

main subject

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author

Klaus Brusgaard

2

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5 July 2017

Kjeldsen AD

1

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5 July 2017

Poulsen L

3

1 reference

5 July 2017

Kruse T

4

1 reference

5 July 2017

Rasmussen K

5

1 reference

5 July 2017

Green A

6

1 reference

5 July 2017

Vase P

7

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5 July 2017

publication date

1 February 2001

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American Journal of Medical Genetics Part A

5 July 2017

published in

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5 July 2017

volume

98

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5 July 2017

issue

4

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5 July 2017

page(s)

298-302

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Clinical heterogeneity in hereditary haemorrhagic telangiectasia: are pulmonary arteriovenous malformations more common in families linked to endoglin?

5 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820010201%2998%3A4%3C298%3A%3AAID-AJMG1093%3E3.0.CO%3B2-K

The activin receptor-like kinase 1 gene: genomic structure and mutations in hereditary hemorrhagic telangiectasia type 2

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820010201%2998%3A4%3C298%3A%3AAID-AJMG1093%3E3.0.CO%3B2-K

Separation of random fragments of DNA according to properties of their sequences

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820010201%2998%3A4%3C298%3A%3AAID-AJMG1093%3E3.0.CO%3B2-K

Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820010201%2998%3A4%3C298%3A%3AAID-AJMG1093%3E3.0.CO%3B2-K

Pulmonary arteriovenous malformations: screening procedures and pulmonary angiography in patients with hereditary hemorrhagic telangiectasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820010201%2998%3A4%3C298%3A%3AAID-AJMG1093%3E3.0.CO%3B2-K

Hereditary haemorrhagic telangiectasia: a population-based study of prevalence and mortality in Danish patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820010201%2998%3A4%3C298%3A%3AAID-AJMG1093%3E3.0.CO%3B2-K

Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820010201%2998%3A4%3C298%3A%3AAID-AJMG1093%3E3.0.CO%3B2-K

Genetic heterogeneity in hereditary haemorrhagic telangiectasia: possible correlation with clinical phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820010201%2998%3A4%3C298%3A%3AAID-AJMG1093%3E3.0.CO%3B2-K

Hereditary haemorrhagic telangiectasia and pulmonary arteriovenous malformations: issues in clinical management and review of pathogenic mechanisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820010201%2998%3A4%3C298%3A%3AAID-AJMG1093%3E3.0.CO%3B2-K

Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome).

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820010201%2998%3A4%3C298%3A%3AAID-AJMG1093%3E3.0.CO%3B2-K

Embolotherapy for Pulmonary Arteriovenous Malformations in Patients with Hereditary Hemorrhagic Telangiectasia (Rendu-Osler-Weber Syndrome)

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820010201%2998%3A4%3C298%3A%3AAID-AJMG1093%3E3.0.CO%3B2-K

10.1002/1096-8628(20010201)98:4<298::AID-AJMG1093>3.0.CO;2-K

21 January 2018

Identifiers

DOI

1 reference

5 July 2017

1 reference