Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
1998-12-23
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
0002-9297
pubmed:author
pubmed:issnType
Print
pubmed:volume
63
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1544-9
pubmed:dateRevised
2008-11-20
pubmed:meshHeading
pubmed-meshheading:9792884-Adolescent, pubmed-meshheading:9792884-Adult, pubmed-meshheading:9792884-Aged, pubmed-meshheading:9792884-Amino Acid Substitution, pubmed-meshheading:9792884-Calcium, pubmed-meshheading:9792884-Child, pubmed-meshheading:9792884-Chromosome Mapping, pubmed-meshheading:9792884-Chromosomes, Human, Pair 11, pubmed-meshheading:9792884-Female, pubmed-meshheading:9792884-Genes, Dominant, pubmed-meshheading:9792884-Humans, pubmed-meshheading:9792884-Hyperparathyroidism, pubmed-meshheading:9792884-Loss of Heterozygosity, pubmed-meshheading:9792884-Male, pubmed-meshheading:9792884-Middle Aged, pubmed-meshheading:9792884-Mutation, Missense, pubmed-meshheading:9792884-Neoplasm Proteins, pubmed-meshheading:9792884-Parathyroid Neoplasms, pubmed-meshheading:9792884-Pedigree, pubmed-meshheading:9792884-Proto-Oncogene Proteins
pubmed:year
1998
pubmed:articleTitle
A family with isolated hyperparathyroidism segregating a missense MEN1 mutation and showing loss of the wild-type alleles in the parathyroid tumors.
pubmed:publicationType
Letter, Research Support, Non-U.S. Gov't