Source:http://linkedlifedata.com/resource/pubmed/id/12970648
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2003-9-12
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pubmed:abstractText |
Thrombocytopenia is a common finding in patients with chromosome 22q11.2 deletion syndrome. Patients with chromosome 22q11.2 deletion syndrome (n=112) were analyzed along with 57 age-matched controls. Even after the exclusion of patients with idiopathic thrombocytopenia purpura, the mean platelet count was approximately 70% of the control population.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0022-3476
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
143
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
277-8
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:12970648-Child,
pubmed-meshheading:12970648-Chromosome Deletion,
pubmed-meshheading:12970648-Chromosomes, Human, Pair 22,
pubmed-meshheading:12970648-DiGeorge Syndrome,
pubmed-meshheading:12970648-Humans,
pubmed-meshheading:12970648-Retrospective Studies,
pubmed-meshheading:12970648-Syndrome,
pubmed-meshheading:12970648-Thrombocytopenia
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pubmed:year |
2003
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pubmed:articleTitle |
Thrombocytopenia in patients with chromosome 22q11.2 deletion syndrome.
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pubmed:affiliation |
Division of Allergy and Immunology, Division of Clinical Genetics, Children's Hospital of Philadelphia, 34th Street and Civic Center Boulevard, Philadelphia, PA 19104, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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