Lin, H <br/><br/>
A frequent deletion polymorphism on chromosome 22q13 identified by representational difference analysis of ovarian cancer.  [electronic resource] 

 -  Genomics  Nov 2000 
 - 391-4 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0888-7543 
<br/><br/><label>Standard No.: </label>10.1006/geno.2000.6357  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Base Sequence<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 22<br/>DNA, Neoplasm<br/>Female<br/>Gene Frequency<br/>Genetic Techniques<br/>Humans<br/>Loss of Heterozygosity<br/>Molecular Sequence Data<br/>Nucleic Acid Conformation<br/>Ovarian Neoplasms--genetics<br/>Polymorphism, Genetic<br/>Tumor Cells, Cultured