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Article

Autosomal dominant exudative vitreoretinopathy: linkage analysis and its clinical application.

German journal of ophthalmology - 1 Jan 1995

Fuhrmann C, Duvigneau C, Müller B, Schwinger E, Julier C, Laqua H, Gal A

Abstract excerpt

Close linkage without recombination (Zmax = 7.383 at Theta = 0.00) was found between the locus for autosomal dominant exudative vitreoretinopathy (Criswick-Schepens) and the locus D11S388 in 11q14.3-q21. We report on the application of data from linkage studies in the diagnostic management of this disease. To determine the disease risk for two newborn children of two affected mothers more precisely, indirect...

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

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PMID: 7728109

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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.

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Autosomal dominant exudative vitreoretinopathy: linkage analysis and its clinical application.PMID 7728109Read ↗

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Familial exudative vitreoretinopathy linked to D11S533 in a large Asian family with consanguinity.Semantic proximity Read ↗

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

Identification of a recurrent missense mutation in the Norrie disease gene associated with a simplex case of exudative vitreoretinopathy.Semantic proximity Read ↗

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

[Criswick-Schepens syndrome -- familial exudative vitreoretinopathy. Report of six cases in two consanguineous families].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 ↗

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