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Article

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

American journal of medical genetics. Part A - 15 Nov 2005

Spruijt Liesbeth, Verdyck Pieter, Van Hul Wim, Wuyts Wim, de Die-Smulders Christine

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Source

Identifiers

PMID: 16222674
DOI: 10.1002/ajmg.a.30923

Genes

MSX2

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

Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

A novel mutation in the MSX2 gene in a family with foramina parietalia permagna (FPP).PMID 16222674Read ↗

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

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

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

Syndromic 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 ↗

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

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

AP1S2 is mutated in X-linked Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizures (Pettigrew syndrome).Semantic proximity Read ↗

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

SPG2 mimicking multiple sclerosis in a family identified using next generation sequencing.Semantic proximity Read ↗

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