(Q55671012)

13

object named as

Xavier Jeunemaitre

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author name string

Philippe Khau Van Kien

1

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Jean-Eric Wolf

2

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Flavie Mathieu

3

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Limin Zhu

4

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Nicolas Salve

5

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Caroline Bonnet

7

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Gaëtan Lesca

8

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Henri Plauchu

9

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Arnaud Dellinger

10

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Annie Nivelon-Chevallier

11

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François Brunotte

European Journal of Human Genetics

12

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language of work or name

English

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publication date

March 2004

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published in

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volume

12

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issue

3

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page(s)

173-80

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exact match

https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201119

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cites work

Thoracic and thoracoabdominal aortic aneurysm and dissection: an investigation based on autopsy

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201119

Familial patterns of thoracic aortic aneurysms.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201119

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201119

Mapping a locus for familial thoracic aortic aneurysms and dissections (TAAD2) to 3p24-25.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201119

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201119

Two-dimensional echocardiographic aortic root dimensions in normal children and adults

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201119

Regressive logistic models for familial disease and other binary traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201119

A General Model for the Genetic Analysis of Pedigree Data

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201119

Molecular determinants of atrial and ventricular septal defects and patent ductus arteriosus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201119

Strategies for multilocus linkage analysis in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201119

Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201119

Idiopathic Dilatation of the Aorta with Dissection in a Family without Marfan Syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201119

Novel TFAP2B mutations that cause Char syndrome provide a genotype-phenotype correlation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201119

Finding genetic contributions to sporadic disease: a recessive locus at 12q24 commonly contributes to patent ductus arteriosus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201119

A second-generation linkage map of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201119

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201119

Fine-mapping of the spinal muscular atrophy locus to a region flanked by MAP1B and D5S6.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201119

A Single Base Mutation in Type III Procollagen That Converts the Codon for Glycine 619 to Arginine in a Family with Familial Aneurysms and Mild Bleeding Tendencies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201119

Epidemiology and clinicopathology of aortic dissection

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201119

7 January 2021

Fibrillin-1 (FBN1) mutations in patients with thoracic aortic aneurysms

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201119

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/10.1038%2FSJ.EJHG.5201119

7 January 2021

Aortic dissection and patent ductus arteriosus in three generations

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201119

7 January 2021

Reference values for normal adult transesophageal echocardiographic measurements

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201119

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201119

7 January 2021

Familial patent ductus arteriosus and bicuspid aortic valve with hand anomalies: a novel heart-hand syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201119

7 January 2021

Risk factors for aortic dissection: a necropsy study of 161 cases

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201119

7 January 2021

Aorta and aortic valve morphologies predisposing to aortic dissection. An in vivo assessment with transoesophageal echocardiography

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201119

7 January 2021

Noonan syndrome and aortic coarctation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201119

7 January 2021

A 15 base-pair AT-rich variable number tandem repeat in the type III procollagen gene (COL3A1) as an informative marker for 2q31-2q32.3

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201119

7 January 2021