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Article

Refinement of the deletion in 7q21.3 associated with split hand/foot malformation type 1 and Mondini dysplasia.

Journal of medical genetics - 1 May 2004

Wieland I, Muschke P, Jakubiczka S, Volleth M, Freigang B, Wieacker P F

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Topics

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Share to Abnormalities, Multiple
Share to Chromosome Deletion
Share to Chromosomes, Human, Pair 7
Share to Deafness

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

Share to Ear, Inner

Share to Foot Deformities, Congenital

Share to Hand Deformities, Congenital

Share to Hearing Loss, Sensorineural

Source

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Identifiers

PMID: 15121782
DOI: 10.1136/jmg.2003.010587
PMCID: PMC1735762

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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.

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Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

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Refinement of the deletion in 7q21.3 associated with split hand/foot malformation type 1 and Mondini dysplasia.PMID 15121782Read ↗

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Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb developmentSemantic proximity Read ↗

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