Linked Life Data

12960218

Source:http://linkedlifedata.com/resource/pubmed/id/12960218

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
9
pubmed:dateCreated
2003-9-8
pubmed:databankReference
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
1468-6244
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
40
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
704-8
pubmed:dateRevised
2008-11-20
pubmed:meshHeading
pubmed-meshheading:12960218-Abnormalities, Multiple, pubmed-meshheading:12960218-Adolescent, pubmed-meshheading:12960218-Adult, pubmed-meshheading:12960218-Child, pubmed-meshheading:12960218-Child, Preschool, pubmed-meshheading:12960218-DNA, pubmed-meshheading:12960218-DNA Mutational Analysis, pubmed-meshheading:12960218-Developmental Disabilities, pubmed-meshheading:12960218-Family Health, pubmed-meshheading:12960218-Female, pubmed-meshheading:12960218-Genotype, pubmed-meshheading:12960218-Growth Disorders, pubmed-meshheading:12960218-Heart Defects, Congenital, pubmed-meshheading:12960218-Humans, pubmed-meshheading:12960218-Infant, pubmed-meshheading:12960218-Intracellular Signaling Peptides and Proteins, pubmed-meshheading:12960218-Lentigo, pubmed-meshheading:12960218-Male, pubmed-meshheading:12960218-Mutation, pubmed-meshheading:12960218-Noonan Syndrome, pubmed-meshheading:12960218-Pedigree, pubmed-meshheading:12960218-Phenotype, pubmed-meshheading:12960218-Polymorphism, Single-Stranded Conformational, pubmed-meshheading:12960218-Protein Tyrosine Phosphatase, Non-Receptor Type 11, pubmed-meshheading:12960218-Protein Tyrosine Phosphatases, pubmed-meshheading:12960218-Syndrome
pubmed:year
2003
pubmed:articleTitle
Correlation between PTPN11 gene mutations and congenital heart defects in Noonan and LEOPARD syndromes.
pubmed:publicationType
Letter, Research Support, Non-U.S. Gov't