Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
2011-3-9
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
1098-2264
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
50
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
370-3
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:21294210-Adolescent, pubmed-meshheading:21294210-Adult, pubmed-meshheading:21294210-Aged, pubmed-meshheading:21294210-Allelic Imbalance, pubmed-meshheading:21294210-Axin Protein, pubmed-meshheading:21294210-Cohort Studies, pubmed-meshheading:21294210-Cytoskeletal Proteins, pubmed-meshheading:21294210-Female, pubmed-meshheading:21294210-Gene Frequency, pubmed-meshheading:21294210-Germ-Line Mutation, pubmed-meshheading:21294210-Heterozygote Detection, pubmed-meshheading:21294210-Humans, pubmed-meshheading:21294210-Male, pubmed-meshheading:21294210-Melanoma, pubmed-meshheading:21294210-Pedigree, pubmed-meshheading:21294210-Polymorphism, Genetic, pubmed-meshheading:21294210-Rome, pubmed-meshheading:21294210-Wnt Proteins, pubmed-meshheading:21294210-Young Adult, pubmed-meshheading:21294210-beta Catenin
pubmed:year
2011
pubmed:articleTitle
AXIN2 germline mutations are rare in familial melanoma.
pubmed:publicationType
Letter, Comment, Research Support, Non-U.S. Gov't