[Risk assessment for familial occurrence of breast cancer].

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Back to search

Article

[Risk assessment for familial occurrence of breast cancer].

Zentralblatt fur Gynakologie - 1 Jan 1995

Chang-Claude J, Becher H, Hamann U, Schroeder-Kurth T

Abstract excerpt

There is now unequivocal evidence that an estimated 5% of breast cancer cases is inherited in families. Inherited predisposition of cancer in these families is thought to be the result of a mutation in one of several highly penetrant autosomal dominant genes such as BRCA1 or BRCA2. The BRCA1 gene...

Topics

Adult
Aged
BRCA1 Protein
BRCA2 Protein
Breast Neoplasms
Chromosome Aberrations
Chromosome Disorders
Chromosomes, Human, Pair 13
Chromosomes, Human, Pair 17
Female
Genetic Counseling
Genetic Testing
Humans
Middle Aged
Neoplasm Proteins
Neoplastic Syndromes, Hereditary
Pedigree
Phenotype

Source

Open in PubMed

Identifiers

PMID: 7571905

Genes

BRCA1
BRCA2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-7571905-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

discussions

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics