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

Split hand/foot malformation syndrome (SHFM): rare congenital orthopaedic disorder.

BMJ case reports - 27 Jun 2014

Patel Ankur, Sharma Deepak, Yadav Jaivinder, Garg Eva

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Limb Deformities, Congenital
Share to Mutation
Share to Syndrome

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Transcription Factors

Share to Tumor Suppressor Proteins

Source

Open in PubMed Open full text

Identifiers

PMID: 24973351
DOI: 10.1136/bcr-2014-204731
PMCID: PMC4078436

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Split hand/foot malformation syndrome (SHFM): rare congenital orthopaedic disorder.PMID 24973351Read ↗

Insights into the pathogenesis and treatment of split/hand foot malformation (cleft hand/foot)Semantic proximity Read ↗

Split Hand Foot Malformation (SHFM)Semantic proximity Read ↗

Clinical, genetic, and molecular aspects of split-hand/foot malformation: an update.Semantic proximity Read ↗

The expanding panorama of split hand foot malformation.Semantic proximity Read ↗

Split-hand/foot malformation - molecular cause and implications in genetic counseling.Semantic proximity Read ↗

Discrepancies in upper and lower limb patterning in split hand foot malformation.Semantic proximity Read ↗

Split Hand-Foot Malformations-Unveiling Unique Molecular Diagnosis From a Brazilian Cohort.Semantic proximity Read ↗

Metatarsal bony syndactyly in 2 fetuses with Smith-Lemli-Opitz syndrome: An under-recognized part of the clinical spectrum.Semantic proximity Read ↗

Triphalangeal thumb in association with split hand/foot: a phenotypic marker for SHFM3?Semantic proximity Read ↗

Central ray deficiency with extensive syndactyly: a dilemma for classification.Semantic proximity Read ↗

Ehler's Danlos syndrome with atypical foot deformity.Semantic proximity Read ↗

Molecular Genetic Characterization of a Chinese Family with Severe Split Hand/Foot Malformation.Semantic proximity Read ↗

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