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

HOXD10 M319K mutation in a family with isolated congenital vertical talus.

Journal of orthopaedic research : official publication of the Orthopaedic Research Society - 1 Mar 2006

Dobbs Matthew B, Gurnett Christina A, Pierce Brandon, Exner G Ulrich, Robarge Jason, Morcuende Jose A, Cole William G, Templeton Peter A, Foster Bruce, Bowcock Anne M

Abstract excerpt

Congenital vertical talus (CVT) is a primary dislocation of the talonavicular joint that often occurs in neuromusculoskeletal syndromes, but may also be seen as an isolated abnormality. Six families with isolated CVT were ascertained. DNA was isolated from 21 affected individuals and 17 unaffecte...

Read the complete abstract on PubMed

Topics

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

Share to Chromosomes, Human, Pair 2
Share to DNA Mutational Analysis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Foot Deformities, Congenital

Share to Genetic Linkage

Share to Homeodomain Proteins

Share to Mutation, Missense

Share to Transcription Factors

Share to White People

Source

Identifiers

PMID: 16450407
DOI: 10.1002/jor.20052

Genes

HOXD10

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-16450407-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 10 closest

HOXD10 M319K mutation in a family with isolated congenital vertical talus.PMID 16450407Read ↗

Variable hand and foot abnormalities in family with congenital vertical talus and CDMP-1 gene mutation.Semantic proximity Read ↗

Absence of HOXD10 mutations in idiopathic clubfoot and sporadic vertical talus.Semantic proximity Read ↗

A HOX Gene Mutation in a Family with Isolated Congenital Vertical Talus and Charcot-Marie-Tooth DiseaseSemantic proximity Read ↗

Deletions of 5' HOXC genes are associated with lower extremity malformations, including clubfoot and vertical talus.Semantic proximity Read ↗

Skeletal muscle abnormalities and genetic factors related to vertical talus.Semantic proximity Read ↗

Identification and Functional Verification of Variants Associated With Clubfoot and Arthrogrypotic Hand Deformation in a Multigeneration Polish Family.Semantic proximity Read ↗

Skeletal muscle contractile gene (TNNT3, MYH3, TPM2) mutations not found in vertical talus or clubfoot.Semantic proximity Read ↗

Genome-wide meta-analysis identified novel variant associated with hallux valgus in Caucasians.Semantic proximity Read ↗

Variation in CASP10 gene is associated with idiopathic talipes equinovarus.Semantic proximity Read ↗

Narrowing the critical region for congenital vertical talus in patients with interstitial 18q deletions.Semantic proximity Read ↗

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