Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2011-8-11
pubmed:abstractText
The relation with SNF5 mutation and chromosome 22 abnormalities is not clear in hematological neoplasms.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
1421-9662
pubmed:author
pubmed:copyrightInfo
Copyright © 2011 S. Karger AG, Basel.
pubmed:issnType
Electronic
pubmed:volume
126
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
69-75
pubmed:meshHeading
pubmed-meshheading:21494030-Adult, pubmed-meshheading:21494030-Aged, pubmed-meshheading:21494030-Blast Crisis, pubmed-meshheading:21494030-Chromosomal Proteins, Non-Histone, pubmed-meshheading:21494030-Chromosome Aberrations, pubmed-meshheading:21494030-Chromosomes, Human, Pair 22, pubmed-meshheading:21494030-Cytogenetic Analysis, pubmed-meshheading:21494030-DNA-Binding Proteins, pubmed-meshheading:21494030-Female, pubmed-meshheading:21494030-Genetic Association Studies, pubmed-meshheading:21494030-Hematologic Neoplasms, pubmed-meshheading:21494030-Humans, pubmed-meshheading:21494030-In Situ Hybridization, Fluorescence, pubmed-meshheading:21494030-Japan, pubmed-meshheading:21494030-Leukemia, Myeloid, Chronic-Phase, pubmed-meshheading:21494030-Loss of Heterozygosity, pubmed-meshheading:21494030-Male, pubmed-meshheading:21494030-Middle Aged, pubmed-meshheading:21494030-Multiple Myeloma, pubmed-meshheading:21494030-Polymorphism, Genetic, pubmed-meshheading:21494030-Polymorphism, Single-Stranded Conformational, pubmed-meshheading:21494030-Transcription Factors
pubmed:year
2011
pubmed:articleTitle
Absence of mutations on the SNF5 gene in hematological neoplasms with chromosome 22 abnormalities.
pubmed:affiliation
Department of Hematology, Tokyo Women's Medical University, Tokyo, Japan. mori@dh.twmu.ac.jp
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't