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Article

Segregation of two BRCA1 mutations in a single family.

American journal of human genetics - 1 Aug 1996

Stoppa-Lyonnet D, Fricker J P, Essioux L, Pages S, Limacher J M, Sobol H, Laurent-Puig P, Thomas G

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

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Source

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Identifiers

PMID: 8755940
PMCID: PMC1914743

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.

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

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Segregation of two BRCA1 mutations in a single family.PMID 8755940Read ↗

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Double heterozygotes for the Ashkenazi founder mutations in BRCA1 and BRCA2 genes.Semantic proximity Read ↗

Phenotypic expression of double heterozygosity for BRCA1 and BRCA2 germline mutations.Semantic proximity Read ↗

The segregation of cancer-causing genes in human populations.Semantic proximity Read ↗

Familial breast cancer: double heterozygosity for BRCA1 and BRCA2 mutations with differing phenotypes.Semantic proximity Read ↗

Cancer aggregation and complex segregation analysis of families with female non-smoking lung cancer probands in TaiwanSemantic proximity Read ↗

Of mice and (wo)men: genotype-phenotype correlations in BRCA1.Semantic proximity Read ↗

A SImplified method for Segregation Analysis (SISA) to determine penetrance and expression of a genetic variant in a family.Semantic proximity Read ↗

Genetic analysis of eight breast-ovarian cancer families with suspected BRCA1 mutations.Semantic proximity Read ↗

Elucidation of the transmission of a novel mutation in BRCA1 (1125delCT) in a family with multiple cases of breast cancer.Semantic proximity Read ↗

BRCA2: breaks, mistakes and failed separations.Semantic proximity Read ↗

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