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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
|
pubmed:dateCreated |
1995-3-16
|
pubmed:commentsCorrections | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:issn |
0277-0938
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
14
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1055-7
|
pubmed:dateRevised |
2004-11-17
|
pubmed:meshHeading |
pubmed-meshheading:7855008-Acute Disease,
pubmed-meshheading:7855008-Amino Acid Metabolism, Inborn Errors,
pubmed-meshheading:7855008-Cells, Cultured,
pubmed-meshheading:7855008-Child, Preschool,
pubmed-meshheading:7855008-Chromosome Aberrations,
pubmed-meshheading:7855008-Female,
pubmed-meshheading:7855008-Humans,
pubmed-meshheading:7855008-Tyrosine
|
pubmed:articleTitle |
Chromosomal instability in hereditary tyrosinemia type I.
|
pubmed:publicationType |
Letter,
Comment,
Case Reports
|