Linked Life Data

19460271

Source:http://linkedlifedata.com/resource/pubmed/id/19460271

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2009-5-22
pubmed:abstractText
Bruck syndrome is characterised by osteogenesis imperfecta and arthrogryposis multiplex. In some patients, mutations in the lysyl hydroxylase 2 gene (PLOD2, 3q23-q24) have been demonstrated. A male newborn with Bruck syndrome is reported.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
1465-3281
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
29
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
159-62
pubmed:meshHeading
pubmed:year
2009
pubmed:articleTitle
Bruck syndrome: osteogenesis imperfecta and arthrogryposis multiplex congenita.
pubmed:affiliation
Division of Neonatology, Department of Pediatrics, Faculty of Medicine, Cukurova University, Adana, Turkey. yyhacer@hotmail.com
pubmed:publicationType
Journal Article, Case Reports