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

The Otto Aufranc Award: Identification of a 4 Mb region on chromosome 17q21 linked to developmental dysplasia of the hip in one 18-member, multigeneration family.

Clinical orthopaedics and related research - 1 Feb 2010

Feldman George, Dalsey Chelsea, Fertala Kasia, Azimi David, Fortina Paolo, Devoto Marcella, Pacifici Maurizio, Parvizi Javad

Abstract excerpt

Developmental dysplasia of the hip (DDH) is a disabling condition that, depending on geography, can afflict between 20% and 80% of patients with end-stage arthritis of the hip. Despite its prevalence, the etiology of this disease remains unknown. DDH is a complex disorder with both environmental and genetic causes. Based on the literature the candidate genes for the disease are HOXB9, collagen type I alpha1, and...

Read the complete abstract on PubMed

Topics

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

Share to Chromosomes, Human, Pair 17
Share to Haplotypes

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

Share to Hip Dislocation, Congenital

Share to Hip Joint

Share to Lod Score

Share to Oligonucleotide Array Sequence Analysis

Share to Radiography

Share to Severity of Illness Index

Source

Open in PubMed Open full text

Identifiers

PMID: 19756907
DOI: 10.1007/s11999-009-1073-6
PMCID: PMC2807013

Genes

HOXB9

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

The Otto Aufranc Award: Identification of a 4 Mb region on chromosome 17q21 linked to developmental dysplasia of the hip in one 18-member, multigeneration family.PMID 19756907Read ↗

Genetics of developmental dysplasia of the hip.Semantic proximity Read ↗

Genetic study identifies novel genes in developmental dysplasia of the hip.Semantic proximity Read ↗

Developmental dysplasia of the hip: usefulness of next generation genomic tools for characterizing the underlying genes - a mini review.Semantic proximity Read ↗

Review of susceptibility genes in developmental dysplasia of the hip: A comprehensive examination of candidate genes and pathways.Semantic proximity Read ↗

Novel mutation in Teneurin 3 found to co‐segregate in all affecteds in a multi‐generation family with developmental dysplasia of the hipSemantic proximity Read ↗

The Genetic Epidemiology of Developmental Dysplasia of the Hip: A Genome-Wide Association Study Harnessing National Clinical Audit DataSemantic proximity Read ↗

Developmental dysplasia of the hip: linkage mapping and whole exome sequencing identify a shared variant in CX3CR1 in all affected members of a large multigeneration family.Semantic proximity Read ↗

Genome-wide association study of developmental dysplasia of the hip identifies an association with GDF5Semantic proximity Read ↗

Molecular mechanisms and genetic factors contributing to the developmental dysplasia of the hipSemantic proximity Read ↗

Whole genome sequencing of pairwise human subjects reveals DNA mutations specific to developmental dysplasia of the hip.Semantic proximity Read ↗

Genetic analysis of a child with 18q Deletion Syndrome and Developmental Dysplasia of HipSemantic proximity Read ↗

Genetic study on developmental dysplasia of the hip.Semantic proximity Read ↗

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