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

Is population bone mineral density variation linked to the marker D11S987 on chromosome 11q12-13?

The Journal of clinical endocrinology and metabolism - 1 Aug 2001

Deng H W, Xu F H, Conway T, Deng X T, Li J L, Davies K M, Deng H, Johnson M, Recker R R

Abstract excerpt

Our purpose is to test linkage of human chromosome 11q12-13 to BMD variation. Chromosome 11q12-13 has been linked to three BMD-related phenotypes that are inherited as Mendelian traits in human pedigrees: an autosomal dominant high bone mass trait, autosomal recessive osteoporosis pseudoglioma, a...

Read the complete abstract on PubMed

Topics

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

Share to Bone Density
Share to Chromosomes, Human, Pair 11
Share to Europe

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Family

Share to Lod Score

Share to Nuclear Family

Share to Odds Ratio

Share to White People

Source

Identifiers

PMID: 11502804
DOI: 10.1210/jcem.86.8.7762

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-11502804-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Is population bone mineral density variation linked to the marker D11S987 on chromosome 11q12-13?PMID 11502804Read ↗

Linkage of a gene causing high bone mass to human chromosome 11 (11q12-13)Semantic proximity Read ↗

Genome screen for QTLs contributing to normal variation in bone mineral density and osteoporosis.Semantic proximity Read ↗

A genome-wide linkage scan for bone mineral density in an extended sample: evidence for linkage on 11q23 and Xq27.Semantic proximity Read ↗

Genome-Wide Linkage Screen of Bone Mineral Density (BMD) in European Pedigrees Ascertained through a Male Relative with Low BMD Values: Evidence for Quantitative Trait Loci on 17q21–23, 11q12–13, 13q12–14, and 22q11Semantic proximity Read ↗

Sibling pair linkage and association studies between peak bone mineral density and the gene locus for the osteoclast-specific subunit (OC116) of the vacuolar proton pump on chromosome 11p12-13.Semantic proximity Read ↗

Osteoporosis-pseudoglioma syndrome, a disorder affecting skeletal strength and vision, is assigned to chromosome region 11q12-13.Semantic proximity Read ↗

Univariate and bivariate variance component linkage analysis of a whole-genome scan for loci contributing to bone mineral density.Semantic proximity Read ↗

First-stage autosomal genome screen in extended pedigrees suggests genes predisposing to low bone mineral density on chromosomes 1p, 2p and 4q.Semantic proximity Read ↗

Genome screen for quantitative trait loci contributing to normal variation in bone mineral density: the Framingham Study.Semantic proximity Read ↗

A whole genome linkage scan for QTLs underlying peak bone mineral density.Semantic proximity Read ↗

Genetic determination of osteoporosis: lessons learned from a large genome-wide linkage study.Semantic proximity Read ↗

Multidimensional Bone Density Phenotyping Reveals New Insights Into Genetic Regulation of the Pediatric Skeleton.Semantic proximity Read ↗

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