(Q34216752)

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Candidate locus analysis of familial ascending aortic aneurysms and dissections confirms the linkage to the chromosome 5q13-14 in Finnish families

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Europe PubMed Central

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31 July 2017

Candidate locus analysis of familial ascending aortic aneurysms and dissections confirms the linkage to the chromosome 5q13-14 in Finnish families (English)

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Europe PubMed Central

PubMed publication ID

31 July 2017

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Juhani Airaksinen

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Juhani Airaksinen

4

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6

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Tatu Juvonen

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31 July 2017

Kaj Groundstroem

5

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Kaj Groundstroem

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31 July 2017

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Sakari Kakko

1

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31 July 2017

Tuija Räisänen

2

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31 July 2017

Minna Tamminen

3

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31 July 2017

Antti Ylitalo

7

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31 July 2017

Paavo Uusimaa

8

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31 July 2017

Markku J Savolainen

9

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31 July 2017

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publication date

1 July 2003

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31 July 2017

The Journal of Thoracic and Cardiovascular Surgery

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31 July 2017

126

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31 July 2017

1

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31 July 2017

106-113

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31 July 2017

Familial patterns of thoracic aortic aneurysms.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-5223%2803%2900037-0

7 January 2021

Familial thoracic aortic dilatations and dissections: a case control study

1 reference

https://api.crossref.org/works/10.1016%2FS0022-5223%2803%2900037-0

7 January 2021

Reduced penetrance and variable expressivity of familial thoracic aortic aneurysms/dissections

1 reference

https://api.crossref.org/works/10.1016%2FS0022-5223%2803%2900037-0

7 January 2021

Mutations in the human gene for fibrillin-1 (FBN1) in the Marfan syndrome and related disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0022-5223%2803%2900037-0

7 January 2021

A second locus for Marfan syndrome maps to chromosome 3p24.2-p25.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-5223%2803%2900037-0

7 January 2021

Familial thoracic aortic aneurysms and dissections: genetic heterogeneity with a major locus mapping to 5q13-14

1 reference

https://api.crossref.org/works/10.1016%2FS0022-5223%2803%2900037-0

7 January 2021

Identification of a chromosome 11q23.2-q24 locus for familial aortic aneurysm disease, a genetically heterogeneous disorder

1 reference

https://api.crossref.org/works/10.1016%2FS0022-5223%2803%2900037-0

7 January 2021

Genetic analysis of MMP3, MMP9, and PAI-1 in Finnish patients with abdominal aortic or intracranial aneurysms

1 reference

https://api.crossref.org/works/10.1016%2FS0022-5223%2803%2900037-0

7 January 2021

Enhanced expression of matrix metalloproteinase-9 in abdominal aortic aneurysms

1 reference

https://api.crossref.org/works/10.1016%2FS0022-5223%2803%2900037-0

7 January 2021

Analysis of coding sequences for tissue inhibitor of metalloproteinases 1 (TIMP1) and 2 (TIMP2) in patients with aneurysms

1 reference

https://api.crossref.org/works/10.1016%2FS0022-5223%2803%2900037-0

7 January 2021

Molecular genetics of the Finnish disease heritage.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-5223%2803%2900037-0

7 January 2021

Report of the American Society of Echocardiography Committee on Nomenclature and Standards in Two-dimensional Echocardiography

1 reference

https://api.crossref.org/works/10.1016%2FS0022-5223%2803%2900037-0

7 January 2021

Echocardiographic reference values for aortic root size: the Framingham Heart Study

1 reference

https://api.crossref.org/works/10.1016%2FS0022-5223%2803%2900037-0

7 January 2021

A molecular approach to the stratification of cardiovascular risk in families with Marfan's syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0022-5223%2803%2900037-0

7 January 2021

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

1 reference

https://api.crossref.org/works/10.1016%2FS0022-5223%2803%2900037-0

7 January 2021

Are aortic aneurysms caused by atherosclerosis?

1 reference

https://api.crossref.org/works/10.1016%2FS0022-5223%2803%2900037-0

7 January 2021

Identifiers

10.1016/S0022-5223(03)00037-0

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Europe PubMed Central

PubMed publication ID

31 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

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