Pearce, S H <br/><br/>
Calcium-sensing receptor mutations in familial benign hypercalcemia and neonatal hyperparathyroidism.  [electronic resource] 

 -  The Journal of clinical investigation  Dec 1995 
 - 2683-92 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0021-9738 
<br/><br/><label>Standard No.: </label>10.1172/JCI118335  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Base Sequence<br/>Calcium--blood<br/>Child<br/>DNA Primers<br/>Female<br/>Genes, Tumor Suppressor<br/>Genetic Carrier Screening<br/>Humans<br/>Hypercalcemia--genetics<br/>Hyperparathyroidism--genetics<br/>Infant, Newborn<br/>Male<br/>Molecular Sequence Data<br/>Mutation<br/>Parathyroid Glands--metabolism<br/>Pedigree<br/>Point Mutation<br/>Polymerase Chain Reaction<br/>Polymorphism, Single-Stranded Conformational<br/>Receptors, Calcium-Sensing<br/>Receptors, Cell Surface--genetics<br/>Reference Values<br/>Restriction Mapping