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Article

Linkage relationship of X-linked juvenile retinoschisis with Xp22.1-p22.3 probes.

American journal of human genetics - 1 Oct 1990

Sieving P A, Bingham E L, Roth M S, Young M R, Boehnke M, Kuo C Y, Ginsburg D

Abstract excerpt

Linkage analysis was performed to evaluate the relationship between the locus for X-linked juvenile retinoschisis (RS) and five X-chromosomal markers-RC8 (DXS9), SE3.2L (DXS16), 99-6 (DXS41), D2 (DXS43), and 782 (DXS85)-all mapped to the interval Xp22.1-p22.3. Seven U.S. families with 56 affected males were studied. No recombinants were found between RS and DXS9 with a maximum lod score (Z) of 4.93 at a...

Topics

DNA Probes
Female
Gene Frequency
Genetic Carrier Screening
Genetic Linkage
Genetic Markers
Humans
Male
Pedigree
Phenotype
Polymorphism, Restriction Fragment Length

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Recombination, Genetic

Retinal Diseases

Sex Chromosome Aberrations

X Chromosome

Source

Open in PubMed Open full text

Identifiers

PMID: 1977307
PMCID: PMC1683777

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 29 Aug 2026. Prepared record publication-1977307-2026-08-29.1. Manifest publication-graph-cohort-2026-08-29.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 29 Aug 2026.

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Linkage relationship of X-linked juvenile retinoschisis with Xp22.1-p22.3 probes.PMID 1977307Read ↗

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