Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
2000-1-6
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
0020-7136
pubmed:author
pubmed:issnType
Print
pubmed:day
10
pubmed:volume
83
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
803-4
pubmed:dateRevised
2007-7-24
pubmed:meshHeading
pubmed-meshheading:10597198-Adult, pubmed-meshheading:10597198-Aged, pubmed-meshheading:10597198-Aged, 80 and over, pubmed-meshheading:10597198-BRCA2 Protein, pubmed-meshheading:10597198-Carcinoma, Squamous Cell, pubmed-meshheading:10597198-Chromosome Mapping, pubmed-meshheading:10597198-Chromosomes, Human, Pair 13, pubmed-meshheading:10597198-DNA Transposable Elements, pubmed-meshheading:10597198-European Continental Ancestry Group, pubmed-meshheading:10597198-Family, pubmed-meshheading:10597198-France, pubmed-meshheading:10597198-Genes, Tumor Suppressor, pubmed-meshheading:10597198-Genetic Markers, pubmed-meshheading:10597198-Head and Neck Neoplasms, pubmed-meshheading:10597198-Heterozygote Detection, pubmed-meshheading:10597198-Humans, pubmed-meshheading:10597198-Jews, pubmed-meshheading:10597198-Laryngeal Neoplasms, pubmed-meshheading:10597198-Loss of Heterozygosity, pubmed-meshheading:10597198-Middle Aged, pubmed-meshheading:10597198-Mutation, pubmed-meshheading:10597198-Neoplasm Proteins, pubmed-meshheading:10597198-Quebec, pubmed-meshheading:10597198-Sequence Deletion, pubmed-meshheading:10597198-Transcription Factors
pubmed:year
1999
pubmed:articleTitle
An absence of founder BRCA2 mutations in individuals with squamous cell carcinoma of the head and neck.
pubmed:publicationType
Letter