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

Exclusion of mutations in TGIF, ALX3, and ALX4 genes in patients with the syndrome of frontonasal dysgenesis, callosal agenesis, basal encephalocele, and eye anomalies.

American journal of medical genetics. Part A - 1 May 2012

Ribeiro-Bicudo Lucilene Arilho, Quiezi Rodrigo G, Guion-Almeida Maria Leine, Legnaro Chiara, Richieri-Costa Antonio

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 Abnormalities, Multiple
Share to Agenesis of Corpus Callosum
Share to Craniofacial Abnormalities

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Encephalocele

Share to Eye Abnormalities

Share to Homeodomain Proteins

Share to Syndrome

Source

Identifiers

PMID: 22496059
DOI: 10.1002/ajmg.a.35305

Genes

ALX3
ALX4

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 8 closest

Exclusion of mutations in TGIF, ALX3, and ALX4 genes in patients with the syndrome of frontonasal dysgenesis, callosal agenesis, basal encephalocele, and eye anomalies.PMID 22496059Read ↗

Novel homozygous ALX4 mutation causing frontonasal dysplasia-2 in a patient with meningoencephalocele.Semantic proximity Read ↗

Mild nasal malformations and parietal foramina caused by homozygous ALX4 mutations.Semantic proximity Read ↗

HHH syndrome associated with callosal agenesis and disordered neuronal migration.Semantic proximity Read ↗

ARX mutation in a boy with transsphenoidal encephalocele and hypopituitarism.Semantic proximity Read ↗

Targeted molecular investigation in patients within the clinical spectrum of Auriculocondylar syndrome.Semantic proximity Read ↗

Expanding the phenotype of UPF3B-related disorder: Case reports and literature review.Semantic proximity Read ↗

Axenfeld-Rieger syndrome: more than meets the eye.Semantic proximity Read ↗

The Molecular Basis of Human Anophthalmia and MicrophthalmiaSemantic proximity Read ↗

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