(Q34000009)

30 July 2017

title

Genetic segregation analysis of familial mitral valve prolapse shows no linkage to fibrillar collagen genes (English)

1 reference

30 July 2017

main subject

mitral valve prolapse

1 reference

Wordsworth P

1

1 reference

30 July 2017

Ogilvie D

2

1 reference

30 July 2017

Akhras F

3

1 reference

30 July 2017

Jackson G

4

1 reference

30 July 2017

Sykes B

5

1 reference

30 July 2017

publication date

1 March 1989

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30 July 2017

published in

British Heart Journal

1 reference

30 July 2017

volume

61

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30 July 2017

issue

3

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30 July 2017

page(s)

300-306

1 reference

A clinical and echocardiographic study of patients with the hypermobility syndrome

30 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216662

Collagen composition of normal and myxomatous human mitral heart valves

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216662

Mitral valve prolapse: harbinger of death or variant of normal?

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216662

Genetics of mitral valve prolapse

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216662

Restriction fragment length polymorphism associated with the pro alpha 2(I) gene of human type I procollagen. Application to a family with an autosomal dominant form of osteogenesis imperfecta

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216662

Familial syndrome of midsystolic click and late systolic murmur

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216662

Mitral valve disease and open heart surgery in osteogenesis imperfecta tarda

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216662

The syndrome associated with midsystolic click and late systolic murmur.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216662

An RFLP associated with the human type III collagen gene (COL3A1).

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216662

Hypervariable 'minisatellite' regions in human DNA.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216662

Detection of a high frequency RsaI polymorphism in the human pro alpha 2(I) collagen gene which is linked to an autosomal dominant form of osteogenesis imperfecta

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216662

An RFLP close to the human collagen I gene COL1A1.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216662

Polymorphism of DNA sequence in the human pro alpha 2(I) collagen gene

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216662

Clinical features and investigative findings in presence of mitral leaflet prolapse. Study of 85 consecutive patients

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216662

Prevalence of Clinical Mitral-Valve Prolapse in 1169 Young Women

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216662

Aortic root dilatation and mitral valve prolapse in Marfan's syndrome: an ECHOCARDIOgraphic study

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216662

Mitral valve prolapse and conduction defects in Ehlers-Danlos syndrome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216662

The floppy mitral valve. Study of incidence, pathology, and complications in surgical, necropsy, and forensic material

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216662

A Prospective Study of Mitral Valvular Prolapse in Young Men

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216662

Inheritance of mitral valve prolapse: effect of age and sex on gene expression.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216662

Echocardiographic detection of mitral valve prolapse. Exclusion of false positive diagnosis and determination of inheritance

29 October 2018

1 reference

12 December 2020

Mitral valve prolapse-click syndrome in twins

1 reference

12 December 2020

Collagen biosynthesis in normal and abnormal human heart valves

1 reference

12 December 2020

Lethal osteogenesis imperfecta and a collagen gene deletion. Length polymorphism provides an alternative explanation

1 reference

12 December 2020

Cardiovascular involvement in osteogenesis imperfecta

1 reference

12 December 2020

Mitral-valve prolapse

1 reference

12 December 2020

Osteogenesis imperfecta is linked to both type I collagen structural genes

1 reference

12 December 2020

Ehlers-Danlos syndrome type IV: cosegregation of the phenotype to a COL3A1 allele of type III procollagen

1 reference

12 December 2020

Identifiers

DOI

10.1136/HRT.61.3.300

1 reference

30 July 2017

1 reference

30 July 2017

1 reference