Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

A dominant Stargardt's macular dystrophy locus maps to chromosome 13q34.

Archives of ophthalmology (Chicago, Ill. : 1960) - 1 Jun 1994

Zhang K, Bither P P, Park R, Donoso L A, Seidman J G, Seidman C E

Abstract excerpt

OBJECTIVE: To identify the chromosomal location of a mutated gene that causes an autosomal dominant Stargardt's macular dystrophy. METHODS: Ocular examinations were performed on 67 members of a large kindred to identify those with macular dystrophy. DNA analyses defined the genotype of all family members at 49 polymorphic loci. Linkage between the gene defect responsible for this macular dystrophy and each...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adolescent
Share to Aged
Share to Chromosome Mapping

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

Share to Genetic Linkage

Share to Genetic Markers

Share to Genotype

Share to Pedigree

Source

Identifiers

PMID: 8002833
DOI: 10.1001/archopht.1994.01090180057035

Provenance

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.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A dominant Stargardt's macular dystrophy locus maps to chromosome 13q34.PMID 8002833Read ↗

A new locus for autosomal dominant stargardt-like disease maps to chromosome 4.Semantic proximity Read ↗

Analysis of 21 Stargardt's disease families confirms a major locus on chromosome 1p with evidence for non-allelic heterogeneity in a minority of cases.Semantic proximity Read ↗

A gene for late-onset fundus flavimaculatus with macular dystrophy maps to chromosome 1p13.Semantic proximity Read ↗

Autosomal dominant Stargardt-like macular dystrophy segregating in a large Canadian family.Semantic proximity Read ↗

Autosomal dominant Stargardt-like macular dystrophy: I. Clinical characterization, longitudinal follow-up, and evidence for a common ancestry in families linked to chromosome 6q14.Semantic proximity Read ↗

Genetic fine mapping of the gene for recessive Stargardt disease.Semantic proximity Read ↗

An autosomal dominant bull's-eye macular dystrophy (MCDR2) that maps to the short arm of chromosome 4.Semantic proximity Read ↗

Genetic linkage of vitelliform macular degeneration (Best's disease) to chromosome 11q13.Semantic proximity Read ↗

Clinical Features of a Stargardt-Like Dominant Progressive Macular Dystrophy With Genetic Linkage to Chromosome 6qSemantic proximity Read ↗

A gene for Stargardt's disease (fundus flavimaculatus) maps to the short arm of chromosome 1Semantic proximity Read ↗

Fine mapping of the Schnyder's crystalline corneal dystrophy locus.Semantic proximity Read ↗

An early-onset autosomal dominant macular dystrophy (MCDR3) resembling North Carolina macular dystrophy maps to chromosome 5.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.