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rdf:type |
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lifeskim:mentions |
|
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pubmed:issue |
9
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pubmed:dateCreated |
2006-11-20
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pubmed:abstractText |
Germline mutations in the BRCA1 and BRCA2 genes are associated with breast cancer, ovarian cancer and other malignancies. Biallelic mutations of BRCA2 are a cause of Fanconi anemia and characteristic childhood cancers. We undertook this study to evaluate the contribution of familial BRCA mutations to childhood cancer in hereditary breast cancer families.
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pubmed:commentsCorrections |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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|
pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
1538-4047
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pubmed:author |
|
|
pubmed:issnType |
Print
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pubmed:volume |
5
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1098-102
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pubmed:meshHeading |
pubmed-meshheading:16931905-Adolescent,
pubmed-meshheading:16931905-Adult,
pubmed-meshheading:16931905-Breast Neoplasms,
pubmed-meshheading:16931905-Child,
pubmed-meshheading:16931905-Child, Preschool,
pubmed-meshheading:16931905-Female,
pubmed-meshheading:16931905-Genes, BRCA1,
pubmed-meshheading:16931905-Genes, BRCA2,
pubmed-meshheading:16931905-Genetic Predisposition to Disease,
pubmed-meshheading:16931905-Germ-Line Mutation,
pubmed-meshheading:16931905-Humans,
pubmed-meshheading:16931905-Male,
pubmed-meshheading:16931905-Neoplasms,
pubmed-meshheading:16931905-Ovarian Neoplasms,
pubmed-meshheading:16931905-Pedigree,
pubmed-meshheading:16931905-Retrospective Studies
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pubmed:year |
2006
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pubmed:articleTitle |
Childhood cancer in families with and without BRCA1 or BRCA2 mutations ascertained at a high-risk breast cancer clinic.
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pubmed:affiliation |
School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, Non-U.S. Gov't
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