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

Sequence variation within the fragile X locus.

Genome research - 1 Aug 2001

Mathews D J, Kashuk C, Brightwell G, Eichler E E, Chakravarti A

Abstract excerpt

The human genome provides a reference sequence, which is a template for resequencing studies that aim to discover and interpret the record of common ancestry that exists in extant genomes. To understand the nature and pattern of variation and linkage disequilibrium comprising this history, we present a study of approximately 31 kb spanning an approximately 70 kb region of FMR1, sequenced in a sample of 20 humans...

Read the complete abstract on PubMed

Topics

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

Share to Fragile X Mental Retardation Protein
Share to Fragile X Syndrome
Share to Gorilla gorilla

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

Share to Linkage Disequilibrium

Share to Nerve Tissue Proteins

Share to Pan troglodytes

Share to Recombination, Genetic

Share to RNA-Binding Proteins

Source

Open in PubMed Open full text

Identifiers

PMID: 11483579
DOI: 10.1101/gr.172601
PMCID: PMC311115

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

Sequence variation within the fragile X locus.PMID 11483579Read ↗

DNA polymorphism in a worldwide sample of human X chromosomes.Semantic proximity Read ↗

Worldwide DNA sequence variation in a 10-kilobase noncoding region on human chromosome 22.Semantic proximity Read ↗

Global patterns of human DNA sequence variation in a 10-kb region on chromosome 1.Semantic proximity Read ↗

FMR1 in global populations.Semantic proximity Read ↗

Gene diversity patterns at 10 X-chromosomal loci in humans and chimpanzees.Semantic proximity Read ↗

A worldwide phylogeography for the human X chromosome.Semantic proximity Read ↗

Human DNA sequence variation in a 6.6-kb region containing the melanocortin 1 receptor promoter.Semantic proximity Read ↗

One in four individuals of African-American ancestry harbors a 5.5kb deletion at chromosome 11q13.1.Semantic proximity Read ↗

Extended gene diversity at the FMR1 locus and neighbouring CA repeats in a sub-Saharan population.Semantic proximity Read ↗

Minisatellite diversity supports a recent African origin for modern humans.Semantic proximity Read ↗

Segments containing alternating purine and pyrimidine dinucleotides: patterns of polymorphism in humans and prevalence throughout phylogeny.Semantic proximity Read ↗

The mitochondrial landscape of African Americans: An examination of more than 2500 control region haplotypes from 22 U.S. locations.Semantic proximity Read ↗

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