New nonsense mutation in the breast cancer-1 gene in a French site-specific breast cancer family.

doi:10.1002/(SICI)1098-1004(1997)9:5<474::AID-HUMU17>3.0.CO;2-#

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

Community

Back to search

Article

New nonsense mutation in the breast cancer-1 gene in a French site-specific breast cancer family.

Human mutation - 1 Jan 1997

Laplace-Marieze V, Presneau N, Girodet C, Vidal V, Vaurs C, Rio P, Bignon Y J

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Aged
Share to Aged, 80 and over
Share to Codon, Terminator
Share to France

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genes, BRCA1

Share to Mutation

Source

Open in PubMed

Identifiers

PMID: 9143931
DOI: 10.1002/(SICI)1098-1004(1997)9:5<474::AID-HUMU17>3.0.CO;2-#

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.

Research trail→

Click a neighbor to travelStep 1 · 8 closest

New nonsense mutation in the breast cancer-1 gene in a French site-specific breast cancer family.PMID 9143931Read ↗

Two contiguously located germline BRCA1 mutations in a Spanish early-onset breast cancer family.Semantic proximity Read ↗

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

A single nucleotide (T-->G) polymorphism within intron 23 of the canine BRCA1 gene.Semantic proximity Read ↗

Unique de novo mutation of BRCA2 in a woman with early onset breast cancer.Semantic proximity Read ↗

Mutations and polymorphisms in the familial early-onset breast cancer (BRCA1) gene. Breast Cancer Information Core.Semantic proximity Read ↗

Novel and common BRCA1 mutations in familial breast/ovarian cancer patients from Lithuania.Semantic proximity Read ↗

[Acquired genetic abnormalities in cancer of the breast].Semantic proximity Read ↗

[Germline mutations and breast cancer risk].Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.