(Q28348819)

5 July 2017

0 references

A new locus for autosomal dominant familial exudative vitreoretinopathy maps to chromosome 11p12-13. (English)

1 reference

exudative vitreoretinopathy

5 July 2017

1 reference

Downey LM

1

1 reference

5 July 2017

Keen TJ

2

1 reference

5 July 2017

Roberts E

3

1 reference

5 July 2017

Mansfield DC

4

1 reference

5 July 2017

Bamashmus M

5

1 reference

5 July 2017

Inglehearn CF

6

1 reference

5 July 2017

language of work or name

English

0 references

publication date

19 January 2001

1 reference

American Journal of Human Genetics

5 July 2017

1 reference

5 July 2017

68

1 reference

5 July 2017

778-781

1 reference

5 July 2017

3

1 reference

Autosomal recessive familial exudative vitreoretinopathy: evidence for genetic heterogeneity

5 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1274490

A mutation in the Norrie disease gene (NDP) associated with X-linked familial exudative vitreoretinopathy

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1274490

Genetic heterogeneity in familial exudative vitreoretinopathy; exclusion of the EVR1 locus on chromosome 11q in a large autosomal dominant pedigree

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1274490

Identification of missense mutations in the Norrie disease gene associated with advanced retinopathy of prematurity

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1274490

Familial exudative vitreoretinopathy

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1274490

X linked exudative vitreoretinopathy: clinical features and genetic linkage analysis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1274490

Linkage and candidate gene analysis of X-linked familial exudative vitreoretinopathy

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1274490

Autosomal dominant exudative vitreoretinopathy

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1274490

The autosomal dominant familial exudative vitreoretinopathy locus maps on 11q and is closely linked to D11S533

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1274490

Norrie disease is caused by mutations in an extracellular protein resembling C-terminal globular domain of mucins

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1274490

Norrie disease gene: characterization of deletions and possible function.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1274490

Retinopathy of prematurity: a new epidemic?

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1274490

Racial variation in retinopathy of prematurity. The Cryotherapy for Retinopathy of Prematurity Cooperative Group.

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1274490

Familial exudative vitreoretinopathy

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1274490

Retinal Vascular Pattern in Familial Exudative Vitreoretinopathy

27 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11179025

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Mapping of the autosomal dominant exudative vitreoretinopathy locus (EVR1) by multipoint linkage analysis in four families

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11179025

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Vascularization of the human fetal retina: roles of vasculogenesis and angiogenesis

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11179025

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1086/318790

1 reference

5 July 2017

1 reference

5 July 2017

1 reference