(Q33403224)

English

Phenotypic overlap of familial exudative vitreoretinopathy (FEVR) with persistent fetal vasculature (PFV) caused by FZD4 mutations in two distinct pedigrees

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scholarly article

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Europe PubMed Central

PubMed publication ID

26 July 2017

Phenotypic overlap of familial exudative vitreoretinopathy (FEVR) with persistent fetal vasculature (PFV) caused by FZD4 mutations in two distinct pedigrees (English)

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

exudative vitreoretinopathy

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inferred from title

author name string

Johane M Robitaille

1

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Karin Wallace

2

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Binyou Zheng

3

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

M Jill Beis

4

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Mark Samuels

5

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Ann Hoskin-Mott

6

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Duane L Guernsey

7

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

publication date

1 March 2009

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Europe PubMed Central

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26 July 2017

Ophthalmic Genetics

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Europe PubMed Central

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26 July 2017

30

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Europe PubMed Central

PubMed publication ID

26 July 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

23-30

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Familial exudative vitreoretinopathy mimicking persistent hyperplastic primary vitreous

1 reference

https://api.crossref.org/works/10.1080%2F13816810802464312

21 January 2018

Familial exudative vitreoretinopathy: surgical intervention and visual acuity outcomes

1 reference

https://api.crossref.org/works/10.1080%2F13816810802464312

21 January 2018

Complexity of the genotype-phenotype correlation in familial exudative vitreoretinopathy with mutations in the LRP5 and/or FZD4 genes

1 reference

https://api.crossref.org/works/10.1080%2F13816810802464312

21 January 2018

Autosomal dominant familial exudative vitreoretinopathy in two Japanese families with FZD4 mutations (H69Y and C181R)

1 reference

https://api.crossref.org/works/10.1080%2F13816810802464312

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1080%2F13816810802464312

21 January 2018

Mutant frizzled-4 disrupts retinal angiogenesis in familial exudative vitreoretinopathy

1 reference

https://api.crossref.org/works/10.1080%2F13816810802464312

21 January 2018

Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinopathy locus on chromosome 11q.

1 reference

https://api.crossref.org/works/10.1080%2F13816810802464312

21 January 2018

Vascular development in the retina and inner ear: control by Norrin and Frizzled-4, a high-affinity ligand-receptor pair

1 reference

https://api.crossref.org/works/10.1080%2F13816810802464312

21 January 2018

Severe form of familial exudative vitreoretinopathy caused by homozygous R417Q mutation in frizzled-4 gene

1 reference

https://api.crossref.org/works/10.1080%2F13816810802464312

21 January 2018

Persistent hyperplastic primary vitreous

1 reference

https://api.crossref.org/works/10.1080%2F13816810802464312

21 January 2018

Teratogenesis of sodium valproate

1 reference

https://api.crossref.org/works/10.1080%2F13816810802464312

21 January 2018

Valproic acid as epigenetic cancer drug: preclinical, clinical and transcriptional effects on solid tumors

1 reference

https://api.crossref.org/works/10.1080%2F13816810802464312

21 January 2018

Reduced bone mineral density and hyaloid vasculature remnants in a consanguineous recessive FEVR family with a mutation in LRP5

1 reference

https://api.crossref.org/works/10.1080%2F13816810802464312

21 January 2018

Frizzled 4 gene (FZD4) mutations in patients with familial exudative vitreoretinopathy with variable expressivity

1 reference

https://api.crossref.org/works/10.1080%2F13816810802464312

21 January 2018

Further evidence of genetic heterogeneity in familial exudative vitreoretinopathy; exclusion of EVR1, EVR3, and EVR4 in a large autosomal dominant pedigree

1 reference

https://api.crossref.org/works/10.1080%2F13816810802464312

21 January 2018

Coats' disease of the retina (unilateral retinal telangiectasis) caused by somatic mutation in the NDP gene: a role for norrin in retinal angiogenesis

1 reference

https://api.crossref.org/works/10.1080%2F13816810802464312

21 January 2018

Norrie gene product is necessary for regression of hyaloid vessels

1 reference

https://api.crossref.org/works/10.1080%2F13816810802464312

21 January 2018

Role of the Norrie disease pseudoglioma gene in sprouting angiogenesis during development of the retinal vasculature

1 reference

https://api.crossref.org/works/10.1080%2F13816810802464312

21 January 2018

Identifiers

10.1080/13816810802464312

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

release_hfpipwkc7fa25ffzznhat34zxa

1 reference

https://api.fatcat.wiki/v0/release/hfpipwkc7fa25ffzznhat34zxa

24 November 2022

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mapped directly with Wikidata item

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

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