Linked Life Data

11288710

Source:http://linkedlifedata.com/resource/pubmed/id/11288710

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2001-4-4
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
1468-6244
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
38
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
113-7
pubmed:dateRevised
2008-11-20
pubmed:meshHeading
pubmed-meshheading:11288710-Abnormalities, Multiple, pubmed-meshheading:11288710-Ataxia Telangiectasia, pubmed-meshheading:11288710-Base Sequence, pubmed-meshheading:11288710-Child, Preschool, pubmed-meshheading:11288710-Chromosome Aberrations, pubmed-meshheading:11288710-Chromosome Breakage, pubmed-meshheading:11288710-DNA, pubmed-meshheading:11288710-DNA Mutational Analysis, pubmed-meshheading:11288710-Female, pubmed-meshheading:11288710-Growth Disorders, pubmed-meshheading:11288710-Humans, pubmed-meshheading:11288710-Microcephaly, pubmed-meshheading:11288710-Mutation, pubmed-meshheading:11288710-Nuclear Proteins, pubmed-meshheading:11288710-Polydactyly, pubmed-meshheading:11288710-Sequence Deletion, pubmed-meshheading:11288710-Syndrome, pubmed-meshheading:11288710-Translocation, Genetic
pubmed:year
2001
pubmed:articleTitle
A novel mutation and novel features in Nijmegen breakage syndrome.
pubmed:publicationType
Letter, Research Support, Non-U.S. Gov't