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Article

Deletion of GLI3 supports the homology of the human Greig cephalopolysyndactyly syndrome (GCPS) and the mouse mutant extra toes (Xt).

Mammalian genome : official journal of the International Mammalian Genome Society - 1 Jan 1992

Vortkamp A, Franz T, Gessler M, Grzeschik K H

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

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Source

Identifiers

PMID: 1322743
DOI: 10.1007/BF00356157

Genes

GLI3

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

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Deletion of GLI3 supports the homology of the human Greig cephalopolysyndactyly syndrome (GCPS) and the mouse mutant extra toes (Xt).PMID 1322743Read ↗

A mouse model of greig cephalopolysyndactyly syndrome: the extra-toesJ mutation contains an intragenic deletion of the Gli3 gene.Semantic proximity Read ↗

Expression of the zinc finger gene Gli3 is affected in the morphogenetic mouse mutant extra-toes (Xt).Semantic proximity Read ↗

High-resolution mapping of the Gli3 mutation extra-toes reveals a 51.5-kb deletion.Semantic proximity Read ↗

Gene symbol: GLI3. Disease: Greig cephalopolysyndactyly syndrome.Semantic proximity Read ↗

Birth defects caused by mutations in human GLI3 and mouse Gli3 genes.Semantic proximity Read ↗

GLI3 ‐related polydactyly: a reviewSemantic proximity Read ↗

What you can learn from one gene: GLI3.Semantic proximity Read ↗

Complex postaxial polydactyly types A and B with camptodactyly, hypoplastic third toe, zygodactyly and other digit anomalies caused by a novel GLI3 mutation.Semantic proximity Read ↗

The clinical atlas of Greig cephalopolysyndactyly syndromeSemantic proximity Read ↗

A novel frameshift mutation GLI3c.1826delG in a Greig-cephalopolysyndactyly syndrome patient with nontypical preaxial polydactyly: A case reportSemantic proximity Read ↗

Novel mutation detection in craniosynostosis promotes characterization, identification, gene expression, tissue engineering and helps clinical practice and translational research.Semantic proximity Read ↗

Novel GLI3 pathogenic variants in complex pre- and postaxial polysyndactyly and Greig cephalopolysyndactyly syndrome.Semantic proximity Read ↗

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