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

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

Mammalian genome : official journal of the International Mammalian Genome Society - 1 Jan 2002

Maynard Thomas M, Jain Michael D, Balmer Curtis W, LaMantia Anthony-Samuel

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 Contig Mapping
Share to Forelimb
Share to Hindlimb
Share to Kruppel-Like Transcription Factors

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

Share to Sequence Homology

Share to Xenopus Proteins

Share to Zinc Finger Protein Gli3

Source

Identifiers

PMID: 11773971
DOI: 10.1007/s00335-001-2115-x

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

High-resolution mapping of the Gli3 mutation extra-toes reveals a 51.5-kb deletion.PMID 11773971Read ↗

The XtJ allele generates a Gli3 fusion transcript.Semantic proximity Read ↗

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

50 Years Ago in TheJournalofPediatrics: Spectrum of GLI3 Mutations.Semantic proximity Read ↗

GLIS1–3 transcription factors: critical roles in the regulation of multiple physiological processes and diseasesSemantic proximity Read ↗

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

The Potential Role of Krüppel-Like Zinc-Finger Protein Glis3 in Genetic Diseases and Cancers.Semantic proximity Read ↗

TALPID3/KIAA0586 regulates multiple aspects of neuromuscular patterning during gastrointestinal development in animal models and humanSemantic proximity Read ↗

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

Molecular genetic characterization of the genomic ACTB-GLI fusion in pericytoma with t(7;12)Semantic proximity Read ↗

Exome sequencing reveals a novel nonsense mutation of GLI3 in a Chinese family with 'non-syndromic' pre-axial polydactyly.Semantic proximity Read ↗

Three new alleles encoding an apparent Kellnull phenotype.Semantic proximity Read ↗

The mouse mutant Polydactyly Nagoya (Pdn) defines a novel allele of the zinc finger gene Gli3.Semantic proximity Read ↗

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