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Article

GLI3 frameshift mutations cause autosomal dominant Pallister-Hall syndrome

1 Mar 1997

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Source

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

Identifiers

PMID: 9054938
DOI: 10.1038/ng0397-266

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

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

Research trail→

Click a neighbor to travelStep 1 · 12 closest

GLI3 frameshift mutations cause autosomal dominant Pallister-Hall syndromePMID 9054938Read ↗

Gene symbol: GLI3. Disease: Pallister-Hall syndrome.Semantic proximity Read ↗

GLI3 ‐related polydactyly: a reviewSemantic proximity Read ↗

Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations.Semantic proximity Read ↗

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

Molecular analysis expands the spectrum of phenotypes associated with GLI3 mutations.Semantic proximity Read ↗

A GLI3 variant leading to polydactyly in heterozygotes and Pallister-Hall-like syndrome in a homozygote.Semantic proximity Read ↗

Pallister-Hall syndrome.Semantic proximity Read ↗

Pallister-Hall syndrome phenotype in mice mutant for Gli3.Semantic proximity Read ↗

GLI3 variants causing isolated polysyndactyly are not restricted to the protein's C-terminal third.Semantic proximity Read ↗

Novel Heterozygous Nonsense GLI2 Mutations in Patients with Hypopituitarism and Ectopic Posterior Pituitary Lobe without HoloprosencephalySemantic proximity Read ↗

Linkage mapping and phenotypic analysis of autosomal dominant Pallister-Hall syndrome.Semantic proximity Read ↗

Pallister-Hall syndrome: unreported skeletal features of a GLI3 mutation.Semantic proximity Read ↗

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