Discover Community Create You

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

Article

Identification of novel intronic BRCA1 variants of uncertain significance in a Thai hereditary breast cancer family.

Journal of genetics - 1 Aug 2011

Ratanaphan Adisorn, Panomwan Pornpen, Canyuk Bhutorn, Maipang Tanaphon

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 Base Pair Mismatch
Share to BRCA1 Protein
Share to Carcinoma, Ductal, Breast
Share to DNA Replication

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hereditary Breast and Ovarian Cancer Syndrome

Share to Nucleic Acid Conformation

Share to Thailand

Share to Trinucleotide Repeats

Source

Identifiers

PMID: 21869484
DOI: 10.1007/s12041-011-0069-7

Genes

BRCA1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Identification of novel intronic BRCA1 variants of uncertain significance in a Thai hereditary breast cancer family.PMID 21869484Read ↗

Analysis of breast cancer susceptibility genes BRCA1 and BRCA2 in Thai familial and isolated early-onset breast and ovarian cancer.Semantic proximity Read ↗

Germline mutations in hereditary breast-ovarian cancer spectrum in Thailand: Results from multi-gene panel testing in 4,567 Thai patientsSemantic proximity Read ↗

BRCA1 disease-associated haplotypes in Singapore Malay women with early-onset breast/ovarian cancer.Semantic proximity Read ↗

Identification of a novel splice-site mutation of the BRCA1 gene in two breast cancer families: screening reveals low frequency in Icelandic breast cancer patients.Semantic proximity Read ↗

BRCA1 c.2845insA is a recurring mutation with a founder effect in Singapore Malay women with early onset breast/ovarian cancer.Semantic proximity Read ↗

BRCA1 c.2845insA is a founder mutation in Singaporean Malay women with early onset breast/ovarian cancer.Semantic proximity Read ↗

Understanding germ-line mutations in BRCA1.Semantic proximity Read ↗

Population-based study of BRCA1 and BRCA2 mutations in 1035 unselected Finnish breast cancer patients.Semantic proximity Read ↗

[Detection of a BRCA1 c.2013_2014ins GT variant an ethnic Han Chinese pedigree affected with breast cancer].Semantic proximity Read ↗

A unique BRCA1 mutation identified in Mongolia.Semantic proximity Read ↗

Emerging roles of BRCA1 alternative splicing.Semantic proximity Read ↗

Splicing analysis of 14 BRCA1 missense variants classifies nine variants as pathogenic.Semantic proximity Read ↗

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