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Article

Holt-Oram syndrome.

The Journal of hand surgery - 1 Aug 2014

Goldfarb Charles A, Wall Lindley B

Abstract excerpt

No abstract is available from the source.

Topics

Abnormalities, Multiple
Genotype
Heart Defects, Congenital
Heart Septal Defects, Atrial
Humans
Lower Extremity Deformities, Congenital
Phenotype
Upper Extremity Deformities, Congenital

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 24656395
DOI: 10.1016/j.jhsa.2014.02.015

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026.

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Related research

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Research trail→

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Holt-Oram syndrome.PMID 24656395Read ↗

Novel TBX5 mutations and molecular mechanism for Holt-Oram syndrome.Semantic proximity Read ↗

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Holt-Oram syndrome: clinical and molecular description of 78 patients with TBX5 variantsSemantic proximity Read ↗

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