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Article

CHEK2 c.1100delC mutation among non-BRCA1/2 Spanish hereditary breast cancer families.

Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico - 1 Feb 2013

Fachal L, Santamariña M, Blanco A, Carracedo A, Vega A

Abstract excerpt

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Topics

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Share to Breast Neoplasms
Share to Checkpoint Kinase 2
Share to Genes, BRCA1
Share to Genes, BRCA2

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Multiplex Polymerase Chain Reaction

Share to Prevalence

Share to Protein Serine-Threonine Kinases

Source

Identifiers

PMID: 23150219
DOI: 10.1007/s12094-012-0967-z

Genes

BRCA1
CHEK2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

CHEK2 c.1100delC mutation among non-BRCA1/2 Spanish hereditary breast cancer families.PMID 23150219Read ↗

Germline CHEK2*1100delC mutations in breast cancer patients with multiple primary cancers.Semantic proximity Read ↗

CHEK2 c.1100delC allele is rarely identified in Greek breast cancer cases.Semantic proximity Read ↗

Interaction between CHEK2*1100delC and other low-penetrance breast-cancer susceptibility genes: a familial studySemantic proximity Read ↗

Role of CHEK2*1100delC in unselected series of non-BRCA1/2 male breast cancers.Semantic proximity Read ↗

Identification of a novel BRCA2 and CHEK2 A-C-G-C haplotype in Turkish patients affected with breast cancer.Semantic proximity Read ↗

A CHEK2 Genetic Variant Contributing to a Substantial Fraction of Familial Breast CancerSemantic proximity Read ↗

[CHEK2-mutation in Dutch breast cancer families: expanding genetic testing for breast cancer].Semantic proximity Read ↗

Cohort profile: a nationwide study in Dutch CHEK2 c.1100delC families using the infrastructure of the HEreditary Breast and Ovarian cancer study Netherlands - Hebon-CHEK2.Semantic proximity Read ↗

Genetic and functional analysis of CHEK2 (CHK2) variants in multiethnic cohorts.Semantic proximity Read ↗

The CHEK2 c.1100delC germline mutation rarely contributes to breast cancer development in the Czech RepublicSemantic proximity Read ↗

Identification of CHEK2 Germline Mutations in BRCA1/2- and PALB2-Negative Breast and Ovarian Cancer Patients.Semantic proximity Read ↗

The CHEK2 1100delC mutation identifies families with a hereditary breast and colorectal cancer phenotype.Semantic proximity Read ↗

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