Bradley, K J <br/><br/>
Parafibromin mutations in hereditary hyperparathyroidism syndromes and parathyroid tumours.  [electronic resource] 

 -  Clinical endocrinology  Mar 2006 
 - 299-306 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0300-0664 
<br/><br/><label>Standard No.: </label>10.1111/j.1365-2265.2006.02460.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Child<br/>DNA, Neoplasm--genetics<br/>Family Health<br/>Female<br/>Gene Frequency<br/>Humans<br/>Hyperparathyroidism--genetics<br/>Jaw Neoplasms--genetics<br/>Loss of Heterozygosity--genetics<br/>Male<br/>Middle Aged<br/>Mutation--genetics<br/>Parathyroid Neoplasms--genetics<br/>Pedigree<br/>Polymorphism, Genetic--genetics<br/>Syndrome<br/>Tumor Suppressor Proteins--genetics