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Article

Interaction between CHEK2*1100delC and other low-penetrance breast-cancer susceptibility genes: a familial study

1 Oct 2005

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 16257342
DOI: 10.1016/s0140-6736(05)67627-1

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Related research

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Click a neighbor to travelStep 1 · 12 closest

Interaction between CHEK2*1100delC and other low-penetrance breast-cancer susceptibility genes: a familial studyPMID 16257342Read ↗

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

A search for modifying genetic factors in CHEK2:c.1100delC breast cancer patients.Semantic proximity Read ↗

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

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

The CHEK2 gene and inherited breast cancer susceptibility.Semantic proximity Read ↗

CHEK2 1100delC variant and breast cancer risk in Caucasians: a meta-analysis based on 25 studies with 29,154 cases and 37,064 controls.Semantic proximity Read ↗

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

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

Genetic modifiers of CHEK2*1100delC-associated breast cancer risk.Semantic proximity Read ↗

The CHEK2*1100delC variant acts as a breast cancer risk modifier in non-BRCA1/BRCA2 multiple-case families.Semantic proximity Read ↗

Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations.Semantic proximity Read ↗

Current perspectives on CHEK2 mutations in breast cancerSemantic proximity Read ↗

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