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Article

Parietal foramina with cleidocranial dysplasia is caused by mutation in MSX2

22 Oct 2003

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 14571277
DOI: 10.1038/sj.ejhg.5201062

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Parietal foramina with cleidocranial dysplasia is caused by mutation in MSX2PMID 14571277Read ↗

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

Cleidocranial dysplasia with severe parietal bone dysplasia: a new (p.Val124Serfs) RUNX2 mutation.Semantic proximity Read ↗

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

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

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

MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans.Semantic proximity Read ↗

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

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

Two Unrelated Families With Noncoding Duplications Upstream of MSX2 Refine the Critical Regulatory Region Likely Involved in Cranial Bone Development and a Cleidocranial Dysplasia-Like Phenotype.Semantic proximity Read ↗

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

Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation.Semantic proximity Read ↗

Cleidocranial Dysplasia with 6p21.1-p12.3 Microdeletion: A Case Report and Literature Review.Semantic proximity Read ↗

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