Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2007-8-22
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
1015-8146
pubmed:author
pubmed:issnType
Print
pubmed:volume
18
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
259-62
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:17710881-Adolescent, pubmed-meshheading:17710881-Aged, pubmed-meshheading:17710881-Chromosome Aberrations, pubmed-meshheading:17710881-Cytoskeletal Proteins, pubmed-meshheading:17710881-DNA Mutational Analysis, pubmed-meshheading:17710881-Familial Mediterranean Fever, pubmed-meshheading:17710881-Female, pubmed-meshheading:17710881-Genes, Dominant, pubmed-meshheading:17710881-Genes, Recessive, pubmed-meshheading:17710881-Heterozygote Detection, pubmed-meshheading:17710881-Homeodomain Proteins, pubmed-meshheading:17710881-Humans, pubmed-meshheading:17710881-Karyotyping, pubmed-meshheading:17710881-LIM-Homeodomain Proteins, pubmed-meshheading:17710881-Male, pubmed-meshheading:17710881-Middle Aged, pubmed-meshheading:17710881-Nail-Patella Syndrome, pubmed-meshheading:17710881-Talus, pubmed-meshheading:17710881-Transcription Factors
pubmed:year
2007
pubmed:articleTitle
Co-occurrence of familial Mediterranean fever (FMF) heterozygote mutation and nail-patella syndrome (NPS) in 3 members of a family with LMX1B mutation analysis.
pubmed:publicationType
Letter, Case Reports