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Article

MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans.

Nature genetics - 1 Apr 2000

van den Boogaard M J, Dorland M, Beemer F A, van Amstel H K

Abstract excerpt

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Topics

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Share to Anodontia
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 10742093
DOI: 10.1038/74155

Genes

MSX1

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

MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans.PMID 10742093Read ↗

MSX1 and orofacial clefting with and without tooth agenesis.Semantic proximity Read ↗

Orodental malformations associated with human MSX1 sequence variants.Semantic proximity Read ↗

Molecular basis of non-syndromic tooth agenesis: mutations of MSX1 and PAX9 reflect their role in patterning human dentition.Semantic proximity Read ↗

A novel frameshift MSX1 mutation in a Saudi family with autosomal dominant premolar and third molar agenesis.Semantic proximity Read ↗

Novel nonsense mutation in MSX1 causes tooth agenesis with cleft lip in a Chinese family.Semantic proximity Read ↗

A novel MSX1 intronic mutation associated with autosomal dominant non-syndromic oligodontia in a large Chinese family pedigree.Semantic proximity Read ↗

MSX1 mutations and associated disease phenotypes: genotype-phenotype relations.Semantic proximity Read ↗

The role of MSX1 in tooth agenesis in Iranians.Semantic proximity Read ↗

Novel human mutation and CRISPR/Cas genome-edited mice reveal the importance of C-terminal domain of MSX1 in tooth and palate development.Semantic proximity Read ↗

Mutations in MSX1, PAX9 and MMP20 genes in Saudi Arabian patients with tooth agenesis.Semantic proximity Read ↗

Novel MSX1 mutation in a family with autosomal-dominant hypodontia of second premolars and third molars.Semantic proximity Read ↗

A human MSX1 homeodomain missense mutation causes selective tooth agenesis.Semantic proximity Read ↗

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