| pubmed-article:9818897 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:9818897 | lifeskim:mentions | umls-concept:C0266464 | lld:lifeskim |
| pubmed-article:9818897 | lifeskim:mentions | umls-concept:C0008665 | lld:lifeskim |
| pubmed-article:9818897 | lifeskim:mentions | umls-concept:C0039082 | lld:lifeskim |
| pubmed-article:9818897 | pubmed:issue | 5 | lld:pubmed |
| pubmed-article:9818897 | pubmed:dateCreated | 1998-12-3 | lld:pubmed |
| pubmed-article:9818897 | pubmed:abstractText | We report two children with chromosome 22q11 deletion syndrome who had neuroradiologic evidence of polymicrogyria. The diagnosis of chromosome 22q11 deletion should be considered in individuals with polymicrogyria. | lld:pubmed |
| pubmed-article:9818897 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9818897 | pubmed:language | eng | lld:pubmed |
| pubmed-article:9818897 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9818897 | pubmed:citationSubset | AIM | lld:pubmed |
| pubmed-article:9818897 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:9818897 | pubmed:month | Nov | lld:pubmed |
| pubmed-article:9818897 | pubmed:issn | 0028-3878 | lld:pubmed |
| pubmed-article:9818897 | pubmed:author | pubmed-author:BinghamP MPM | lld:pubmed |
| pubmed-article:9818897 | pubmed:author | pubmed-author:LynchDD | lld:pubmed |
| pubmed-article:9818897 | pubmed:author | pubmed-author:ZackaiEE | lld:pubmed |
| pubmed-article:9818897 | pubmed:author | pubmed-author:McDonald-McGi... | lld:pubmed |
| pubmed-article:9818897 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:9818897 | pubmed:volume | 51 | lld:pubmed |
| pubmed-article:9818897 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:9818897 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:9818897 | pubmed:pagination | 1500-2 | lld:pubmed |
| pubmed-article:9818897 | pubmed:dateRevised | 2007-11-15 | lld:pubmed |
| pubmed-article:9818897 | pubmed:meshHeading | pubmed-meshheading:9818897-... | lld:pubmed |
| pubmed-article:9818897 | pubmed:meshHeading | pubmed-meshheading:9818897-... | lld:pubmed |
| pubmed-article:9818897 | pubmed:meshHeading | pubmed-meshheading:9818897-... | lld:pubmed |
| pubmed-article:9818897 | pubmed:meshHeading | pubmed-meshheading:9818897-... | lld:pubmed |
| pubmed-article:9818897 | pubmed:meshHeading | pubmed-meshheading:9818897-... | lld:pubmed |
| pubmed-article:9818897 | pubmed:meshHeading | pubmed-meshheading:9818897-... | lld:pubmed |
| pubmed-article:9818897 | pubmed:meshHeading | pubmed-meshheading:9818897-... | lld:pubmed |
| pubmed-article:9818897 | pubmed:meshHeading | pubmed-meshheading:9818897-... | lld:pubmed |
| pubmed-article:9818897 | pubmed:meshHeading | pubmed-meshheading:9818897-... | lld:pubmed |
| pubmed-article:9818897 | pubmed:meshHeading | pubmed-meshheading:9818897-... | lld:pubmed |
| pubmed-article:9818897 | pubmed:meshHeading | pubmed-meshheading:9818897-... | lld:pubmed |
| pubmed-article:9818897 | pubmed:meshHeading | pubmed-meshheading:9818897-... | lld:pubmed |
| pubmed-article:9818897 | pubmed:year | 1998 | lld:pubmed |
| pubmed-article:9818897 | pubmed:articleTitle | Polymicrogyria in chromosome 22 delection syndrome. | lld:pubmed |
| pubmed-article:9818897 | pubmed:affiliation | Division of Neurology, Children's Hospital of Philadelphia, PA 19104, USA. | lld:pubmed |
| pubmed-article:9818897 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:9818897 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:9818897 | pubmed:publicationType | Case Reports | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:9818897 | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:9818897 | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:9818897 | lld:pubmed |
