Article

A Novel Mutation in Human PAX9 Causes Molar Oligodontia

2002-02-01

Abstract excerpt

No abstract is available from the source.

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: 35fcf643-4991-5dec-a076-74c14bf4586c
DOI: 10.1177/154405910208100209

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

A Novel Mutation in Human PAX9 Causes Molar OligodontiaDOI 10.1177/154405910208100209Read

Mutation of PAX9 is associated with oligodontia.Semantic proximity Read

Haploinsufficiency of PAX9 is associated with autosomal dominant hypodontiaSemantic proximity Read

A novel mutation in human PAX9 causes molar oligodontia.Semantic 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

Identification of a nonsense mutation in the PAX9 gene in molar oligodontia.Semantic proximity Read

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

Novel missense mutations in PAX9 causing oligodontia.Semantic proximity Read

A novel PAX9 variant in a Chinese family with non-syndromic oligodontia and genotype-phenotype analysis of PAX9variants.Semantic proximity Read

A missense mutation in PAX9 in a family with distinct phenotype of oligodontia.Semantic proximity Read

Analyses of oligodontia phenotypes and genetic etiologies.Semantic proximity Read

The phenotype and genotype of PAX9 mutations causing tooth agenesis.Semantic proximity Read

[Identification of a novel mutation of the PAX9 gene and clinical treatment in a nonsyndromic oligodontia family].Semantic proximity Read