Hatabu, Naomi <br/><br/>
A Familial Case of a Whole Germline CDC73 Deletion Discordant for Primary Hyperparathyroidism.  [electronic resource] 

 -  Hormone research in paediatrics  2019 
 - 56-63 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1663-2826 
<br/><br/><label>Standard No.: </label>10.1159/000495800  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Aged<br/>Family<br/>Female<br/>Gene Deletion<br/>Genetic Diseases, Inborn<br/>Germ-Line Mutation<br/>Humans<br/>Hyperparathyroidism, Primary--genetics<br/>Male<br/>Middle Aged<br/>Penetrance<br/>Tumor Suppressor Proteins--genetics