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Article

Haploinsufficiency of PAX9 is associated with autosomal dominant hypodontia

14 Mar 2002

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 11941488
DOI: 10.1007/s00439-002-0699-1

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Haploinsufficiency of PAX9 is associated with autosomal dominant hypodontiaPMID 11941488Read ↗

Mutation of PAX9 is associated with oligodontia.Semantic proximity Read ↗

A Novel Mutation in Human PAX9 Causes Molar OligodontiaSemantic proximity Read ↗

Novel PAX9 compound heterozygous variants in a Chinese family with non-syndromic oligodontia and genotype-phenotype analysis of PAX9 variants.Semantic proximity Read ↗

PAX9 gene mutations and tooth agenesis: A review.Semantic proximity Read ↗

PAX-9 polymorphism may be a risk factor for hypodontia: a meta-analysis.Semantic proximity Read ↗

PAX9 polymorphisms and susceptibility with sporadic tooth agenesis in Turkish populations: a case-control study.Semantic proximity Read ↗

Novel missense mutations in PAX9 causing oligodontia.Semantic proximity Read ↗

Analyses of oligodontia phenotypes and genetic etiologies.Semantic proximity Read ↗

Functional study of novel PAX9 variants: The paired domain and non-syndromic oligodontia.Semantic proximity Read ↗

Mutations in the PAX9 gene in sporadic oligodontia.Semantic proximity Read ↗

A novel g.-1258G>A mutation in a conserved putative regulatory element of PAX9 is associated with autosomal dominant molar hypodontia.Semantic proximity Read ↗

Detection of novel variant and functional study in a Chinese family with nonsyndromic oligodontia.Semantic proximity Read ↗

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