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

FRAXAC1 and DXS548 polymorphisms in the Chinese population.

American journal of medical genetics - 28 May 1999

Poon P M, Pang C P, Chen Q L, Zhong N, Lai K Y, Lau C H, Wong C K, Brown W T

Abstract excerpt

The fragile X syndrome is the most common inherited form of mental retardation. Haplotype studies using FRAXAC1 and DXS548 polymorphic markers flanking the fragile site have demonstrated linkage disequilibrium at the FMR1 locus. We investigated the association of the FRAXAC1, DXS548 and CGG alleles between normal subjects and mentally retarded (MR) patients of unspecified cause who do have fragile X syndrome. We...

Read the complete abstract on PubMed

Topics

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

Share to China
Share to Fragile X Mental Retardation Protein
Share to Fragile X Syndrome

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

Share to Genetics, Population

Share to Haplotypes

Share to Nerve Tissue Proteins

Share to Polymorphism, Genetic

Share to RNA-Binding Proteins

Source

Identifiers

PMID: 10331593
DOI: 10.1002/(sici)1096-8628(19990528)84:3<208::aid-ajmg8>3.0.co;2-c

Genes

FMR1

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

FRAXAC1 and DXS548 polymorphisms in the Chinese population.PMID 10331593Read ↗

Frequency of the fragile X syndrome in Chinese mentally retarded populations is similar to that in Caucasians.Semantic proximity Read ↗

Distribution of FMR-1 and associated microsatellite alleles in a normal Chinese population.Semantic proximity Read ↗

DXS548/FRAXAC1 haplotypes in fragile X chromosomes in the Brazilian population.Semantic proximity Read ↗

Haplotype and AGG interspersion analysis of FMR1 alleles in a Croatian population: no founder effect detected in patients with fragile X syndrome.Semantic proximity Read ↗

Haplotype analysis of the fragile X syndrome gene FMR1 in the Czech Republic.Semantic proximity Read ↗

Analysis of FMR1 (CGG)(n) alleles and DXS548-FRAXAC1 haplotypes in three European circumpolar populations: traces of genetic relationship with Asia.Semantic proximity Read ↗

Molecular screening of fragile X (FRAXA) and FRAXE mental retardation syndromes in the Hellenic population of Greece and Cyprus: incidence, genetic variation, and stability.Semantic proximity Read ↗

FMR1 CGG repeat patterns and flanking haplotypes in three Asian populations and their relationship with repeat instability.Semantic proximity Read ↗

Origins of the fragile X syndrome mutation.Semantic proximity Read ↗

Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndrome.Semantic proximity Read ↗

Distribution of CGG/GCC repeats at the FMR1 and FMR2 genes in an Indian population with mental retardation of unknown etiology.Semantic proximity Read ↗

Closely linked cis-acting modifier of expansion of the CGG repeat in high risk FMR1 haplotypes.Semantic proximity Read ↗

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