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

A novel mutation in the MSX2 homeobox gene of a family with foramina parietalia permagna, headache and vascular anomaly.

European journal of pediatrics - 1 Oct 2006

Ghassibé Michella, Bernier Vincent, Boon Laurence M, Vikkula Miikka

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 DNA-Binding Proteins
Share to Family Health
Share to Headache

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Homeodomain Proteins

Share to Radiography

Source

Identifiers

PMID: 16642368
DOI: 10.1007/s00431-006-0138-8

Genes

MSX2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A novel mutation in the MSX2 homeobox gene of a family with foramina parietalia permagna, headache and vascular anomaly.PMID 16642368Read ↗

A novel mutation in the MSX2 gene in a family with foramina parietalia permagna (FPP).Semantic proximity Read ↗

Identification of mutations in the MSX2 homeobox gene in families affected with foramina parietalia permagna.Semantic proximity Read ↗

Malformation of cortical and vascular development in one family with parietal foramina determined by an ALX4 homeobox gene mutation.Semantic proximity Read ↗

Foramina parietalia permagna: Clinical radiological evaluation of a Spanish family with an undescribed mutation in the ALX4 gene.Semantic proximity Read ↗

Parietal foramina with cleidocranial dysplasia is caused by mutation in MSX2Semantic proximity Read ↗

The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500).Semantic proximity Read ↗

Enlarged parietal foramina caused by mutations in the homeobox genes ALX4 and MSX2: from genotype to phenotype.Semantic proximity Read ↗

Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects.Semantic proximity Read ↗

Syndromic foramina parietalia permagna.Semantic proximity Read ↗

Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification.Semantic proximity Read ↗

Foramina parietalia permagna: the ins and outs.Semantic proximity Read ↗

Teaching NeuroImages: alternating ptosis and Marcus Gunn jaw-winking phenomenon with PHOX2B mutation.Semantic proximity Read ↗

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