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Article

A polymorphism in intron 2 of the TP53 gene.

Clinical genetics - 1 Aug 1996

DiCioccio R A, Piver M S

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Share to Alleles
Share to Chromosomes, Human, Pair 17
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Share to Genes, p53

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Share to Polymorphism, Single-Stranded Conformational

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Identifiers

PMID: 8937773

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A polymorphism in intron 2 of the TP53 gene.PMID 8937773Read ↗

Identification of a polymorphism in intron 2 of the p53 gene.Semantic proximity Read ↗

An Alu polymorphism intragenic to the TP53 gene.Semantic proximity Read ↗

A tandem CC-->TT transition in the p53 gene of a breast cancer.Semantic proximity Read ↗

HaeIII polymorphism in intron 1 of the human p53 gene.Semantic proximity Read ↗

Duplication polymorphism within the third intron of the p53 gene is a rare event in Japanese population.Semantic proximity Read ↗

Characterization of three new VNTR alleles in the promoter region of the TPMT gene.Semantic proximity Read ↗

An intronic variant in the TP53 gene in a Brazilian woman with breast cancer.Semantic proximity Read ↗

Evaluation of the polymorphisms in the exons 2 to 4 of the TP53 in cervical carcinoma patients from a Brazilian population.Semantic proximity Read ↗

Polymorphic insertion of additional repeat within an area of direct 8 bp tandem repeats in the 5'-untranslated region of the p53R2 gene and cancer risk.Semantic proximity Read ↗

p53 codon 72 polymorphism and type 1 diabetes mellitus.Semantic proximity Read ↗

Evaluation of a polymorphism in intron 2 of the p53 gene in ovarian cancer patients. From the Danish "Malova" Ovarian Cancer Study.Semantic proximity Read ↗

High frequency of a splice mutation in intron 2 of the 21-hydroxylase gene in Russia could be partly explained by a founder effect.Semantic proximity Read ↗

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