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Article

Heterozygous Germline Mutations in the p53 Homolog p63 Are the Cause of EEC Syndrome

1 Oct 1999

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 10535733
DOI: 10.1016/s0092-8674(00)81646-3

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Related research

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Heterozygous Germline Mutations in the p53 Homolog p63 Are the Cause of EEC SyndromePMID 10535733Read ↗

Pattern of p63 mutations and their phenotypes--update.Semantic proximity Read ↗

p63-associated disorders.Semantic proximity Read ↗

A recurrent TP63 mutation causing EEC3 and Rapp-Hodgkin syndromes.Semantic proximity Read ↗

The p63 gene in EEC and other syndromes.Semantic proximity Read ↗

Insertion/Deletion Polymorphisms in the ΔNp63 Promoter Are a Risk Factor for Bladder Exstrophy Epispadias ComplexSemantic proximity Read ↗

A Splice Site Variation in the <i>TP63</i> Gene Leads to Mild Atypical <scp>EEC3</scp> in a Large Chinese FamilySemantic proximity Read ↗

Molecular basis of EEC (ectrodactyly, ectodermal dysplasia, clefting) syndrome: five new mutations in the DNA-binding domain of the TP63 gene and genotype-phenotype correlation.Semantic proximity Read ↗

EEC syndrome with a de novo mutation (c.953g > a) on exon 7 of P63 gene: a case report.Semantic proximity Read ↗

TP63 mutation in a patient with acro-dermo-ungual-lacrimal-tooth syndrome: Additional evidence of molecular overlap of the ADULT and EEC syndromes.Semantic proximity Read ↗

Mutations in the p53 homolog p63: allele-specific developmental syndromes in humans.Semantic proximity Read ↗

Ectodermal dysplasias: the p63 tail.Semantic proximity Read ↗

AEC syndrome caused by heterozygous mutation in the SAM domain of p63 gene.Semantic proximity Read ↗

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