Kainu, T <br/><br/>
Somatic deletions in hereditary breast cancers implicate 13q21 as a putative novel breast cancer susceptibility locus.  [electronic resource] 

 -  Proceedings of the National Academy of Sciences of the United States of America  Aug 2000 
 - 9603-8 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0027-8424 
<br/><br/><label>Standard No.: </label>10.1073/pnas.97.17.9603  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aged<br/>BRCA2 Protein<br/>Breast Neoplasms--genetics<br/>Chromosome Deletion<br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 13--genetics<br/>Disease Progression<br/>Female<br/>Genes, BRCA1--genetics<br/>Genetic Predisposition to Disease--genetics<br/>Genome, Human<br/>Genotype<br/>Germ-Line Mutation--genetics<br/>Haplotypes--genetics<br/>Humans<br/>Hybrid Cells<br/>Lod Score<br/>Male<br/>Middle Aged<br/>Models, Genetic<br/>Neoplasm Proteins--genetics<br/>Nucleic Acid Hybridization<br/>Pedigree<br/>Transcription Factors--genetics