Source:http://linkedlifedata.com/resource/pubmed/id/12888798
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
8
|
| pubmed:dateCreated |
2003-7-30
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:month |
Aug
|
| pubmed:issn |
1359-4184
|
| pubmed:author |
pubmed-author:AielloFF,
pubmed-author:AyalaG FGF,
pubmed-author:CanzianiFF,
pubmed-author:CapeKK,
pubmed-author:ChiavettaVV,
pubmed-author:D' AnnaRR,
pubmed-author:De LeoGG,
pubmed-author:Di RosaPP,
pubmed-author:EliaMM,
pubmed-author:GambinoGG,
pubmed-author:MirisolaMM,
pubmed-author:RomanoVV,
pubmed-author:SeiditaGG
|
| pubmed:issnType |
Print
|
| pubmed:volume |
8
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
716-7
|
| pubmed:dateRevised |
2010-11-18
|
| pubmed:meshHeading | |
| pubmed:year |
2003
|
| pubmed:articleTitle |
Lack of association of HOXA1 and HOXB1 mutations and autism in Sicilian (Italian) patients.
|
| pubmed:publicationType |
Letter
|