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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
1
|
| pubmed:dateCreated |
1980-6-16
|
| pubmed:abstractText |
A boy aged 2 years 8 months presenting the Rubinstein-Taybi Syndrome (RTS) and a history of recurrent gastrointestinal and respiratory infections was studied. Partial deficient cell immunity and intermittent hyperaminoacidemia and aminoaciduria were ascertained. These findings were interpreted as evidence of phenotypic and probably genetic heterogeneity of RTS.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:month |
Jan
|
| pubmed:issn |
0001-656X
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
69
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
123-5
|
| pubmed:dateRevised |
2009-11-11
|
| pubmed:meshHeading |
pubmed-meshheading:7368907-Abnormalities, Multiple,
pubmed-meshheading:7368907-Amino Acids,
pubmed-meshheading:7368907-Child, Preschool,
pubmed-meshheading:7368907-Humans,
pubmed-meshheading:7368907-Immunity, Cellular,
pubmed-meshheading:7368907-Male,
pubmed-meshheading:7368907-Rubinstein-Taybi Syndrome
|
| pubmed:year |
1980
|
| pubmed:articleTitle |
Deficient cell immunity and mild intermittent hyperaminoacidemia in a patient with the Rubinstein-Taybi Syndrome.
|
| pubmed:publicationType |
Journal Article,
Case Reports
|