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Article

High frequency of allelic imbalance at the BRCA1 region on chromosome 17q in both familial and sporadic ductal breast carcinomas.

Journal of the National Cancer Institute - 18 May 1994

Borg A, Zhang Q X, Johannsson O, Olsson H

Abstract excerpt

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Share to Alleles
Share to Breast Neoplasms
Share to Carcinoma, Ductal, Breast
Share to Chromosomes, Human, Pair 17

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

Share to BRCA1 gene

Source

Identifiers

PMID: 8169978
DOI: 10.1093/jnci/86.10.792

Genes

BRCA1

Provenance

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

High frequency of allelic imbalance at the BRCA1 region on chromosome 17q in both familial and sporadic ductal breast carcinomas.PMID 8169978Read ↗

Allelic imbalance in the region of the BRCA1 gene in ductal carcinoma in situ of the breast.Semantic proximity Read ↗

Four regions of allelic imbalance on 17q12-qter associated with high-grade breast tumors.Semantic proximity Read ↗

Evidence for involvement of BRCA1 in sporadic breast carcinomas.Semantic proximity Read ↗

Mutations of the BRCA1 gene in human cancer.Semantic proximity Read ↗

Detailed deletion analysis of sporadic breast tumors defines an interstitial region of allelic loss on 17q25.Semantic proximity Read ↗

Detection of allelic losses on 17q12-q21 chromosomal region in benign lesions and malignant tumors occurring in a familial context.Semantic proximity Read ↗

Abnormal frequencies of alleles in polymorphic markers of the 17q21 region is associated with breast cancer.Semantic proximity Read ↗

Breast cancer incidence, penetrance and survival in probable carriers of BRCA1 gene mutation in families linked to BRCA1 on chromosome 17q12-21.Semantic proximity Read ↗

Mutation analysis of the BRCA1 gene in ovarian cancers.Semantic proximity Read ↗

High frequency of allelic imbalance at chromosome region 16q22-23 in human breast cancer: correlation with high PgR and low S phase.Semantic proximity Read ↗

CGH analysis of familial non-BRCA1/BRCA2 breast tumors and mutation screening of a candidate locus on chromosome 17q11.2-12.Semantic proximity Read ↗

The important molecular markers on chromosome 17 and their clinical impact in breast cancer.Semantic proximity Read ↗

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