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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
3
|
| pubmed:dateCreated |
1991-10-29
|
| pubmed:abstractText |
The genetic inheritance of familial breast cancer is complex and heterogeneous, i.e. it cannot be explained by one major susceptibility gene. It is likely that the chromosomal abnormalities and genetic lesions detected in the inherited syndromes will be implicated in the development of the more common sporadic breast tumours. Study of this important subgroup is essential to advance our understanding of the tumour biology of breast cancer and to develop adequate screening programmes for high risk young women.
|
| pubmed:commentsCorrections | |
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:status |
MEDLINE
|
| pubmed:month |
Jun
|
| pubmed:issn |
0035-8835
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
36
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
147-51
|
| pubmed:dateRevised |
2006-11-15
|
| pubmed:meshHeading |
pubmed-meshheading:1920225-Adult,
pubmed-meshheading:1920225-Breast Neoplasms,
pubmed-meshheading:1920225-Chromosome Aberrations,
pubmed-meshheading:1920225-Chromosome Disorders,
pubmed-meshheading:1920225-Female,
pubmed-meshheading:1920225-Humans,
pubmed-meshheading:1920225-Middle Aged,
pubmed-meshheading:1920225-Oncogenes,
pubmed-meshheading:1920225-Pedigree
|
| pubmed:year |
1991
|
| pubmed:articleTitle |
Familial breast cancer.
|
| pubmed:affiliation |
University of Bristol, Department of Surgery, Bristol Royal Infirmary, UK.
|
| pubmed:publicationType |
Journal Article,
Review,
Research Support, Non-U.S. Gov't
|