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Article

Evidence for genetic heterogeneity in X-linked familial exudative vitreoretinopathy.

Genomics - 1 Sept 1997

Shastry B S, Liu X, Hejtmancik J F, Plager D A, Trese M T

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 9299244
DOI: 10.1006/geno.1997.4863

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

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Evidence for genetic heterogeneity in X-linked familial exudative vitreoretinopathy.PMID 9299244Read ↗

Autosomal recessive familial exudative vitreoretinopathy: evidence for genetic heterogeneitySemantic proximity Read ↗

Genetic evaluation to establish the diagnosis of X-linked familial exudative vitreoretinopathy.Semantic proximity Read ↗

PHENOTYPIC HETEROGENEITY IN A FAMILY WITH X-LINKED FAMILIAL EXUDATIVE VITREORETINOPATHY WITH PREVENTION OF VISUAL LOSS IN AN AFFECTED MALE CHILD WITH LASER TREATMENT IN INFANCY.Semantic proximity Read ↗

Risk allele of the FZD4 gene for familial exudative vitreoretinopathy.Semantic proximity Read ↗

Genetic correlates of proliferative vitreoretinopathy.Semantic proximity Read ↗

Revision of Initial Referral Diagnosis after Genotypic Confirmation of Familial Exudative Vitreoretinopathy.Semantic proximity Read ↗

The clinical and genetic heterogeneity of autosomal dominant cataract.Semantic proximity Read ↗

Is pseudoexfoliation syndrome inherited? A review of genetic and nongenetic factors and a new observationSemantic proximity Read ↗

Linkage and candidate gene analysis of X-linked familial exudative vitreoretinopathy.Semantic proximity Read ↗

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

Mapping studies of an X-linked familial exudative vitreoretinopathy.Semantic proximity Read ↗

Familial retinal detachment associated with COL2A1 exon 2 and FZD4 mutations.Semantic proximity Read ↗

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