Claes, K <br/><br/>
Mutation analysis of the BRCA1 and BRCA2 genes results in the identification of novel and recurrent mutations in 6/16 flemish families with breast and/or ovarian cancer but not in 12 sporadic patients with early-onset disease. Mutations in brief no. 224. Online.  [electronic resource] 

 -  Human mutation  1999 
 - 256 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1059-7794 
<br/><br/><label>Standard No.: </label>10.1002/(SICI)1098-1004(1999)13:3<256::AID-HUMU12>3.0.CO;2-M  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>BRCA1 Protein--genetics<br/>BRCA2 Protein<br/>Belgium<br/>Breast Neoplasms--genetics<br/>DNA Mutational Analysis<br/>Female<br/>Gene Deletion<br/>Heteroduplex Analysis<br/>Humans<br/>Neoplasm Proteins--genetics<br/>Ovarian Neoplasms--genetics<br/>Point Mutation<br/>Transcription Factors--genetics