Teh, B T <br/><br/>
A family with isolated hyperparathyroidism segregating a missense MEN1 mutation and showing loss of the wild-type alleles in the parathyroid tumors.  [electronic resource] 

 -  American journal of human genetics  Nov 1998 
 - 1544-9 p.  digital 
<br/><br/> Publication Type: Letter; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0002-9297 
<br/><br/><label>Standard No.: </label>10.1086/302097  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Aged<br/>Amino Acid Substitution<br/>Calcium--blood<br/>Child<br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 11<br/>Female<br/>Genes, Dominant<br/>Humans<br/>Hyperparathyroidism--genetics<br/>Loss of Heterozygosity<br/>Male<br/>Middle Aged<br/>Mutation, Missense<br/>Neoplasm Proteins--genetics<br/>Parathyroid Neoplasms--genetics<br/>Pedigree<br/>Proto-Oncogene Proteins