pubmed-article:20162868 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:20162868 | lifeskim:mentions | umls-concept:C0021943 | lld:lifeskim |
pubmed-article:20162868 | lifeskim:mentions | umls-concept:C1516516 | lld:lifeskim |
pubmed-article:20162868 | lifeskim:mentions | umls-concept:C1517992 | lld:lifeskim |
pubmed-article:20162868 | lifeskim:mentions | umls-concept:C0752046 | lld:lifeskim |
pubmed-article:20162868 | lifeskim:mentions | umls-concept:C0162789 | lld:lifeskim |
pubmed-article:20162868 | lifeskim:mentions | umls-concept:C1533148 | lld:lifeskim |
pubmed-article:20162868 | pubmed:issue | 4 | lld:pubmed |
pubmed-article:20162868 | pubmed:dateCreated | 2010-2-18 | lld:pubmed |
pubmed-article:20162868 | pubmed:abstractText | Fluorescence In Situ Hybridization and single nucleotide polymorphism of a new case with inv dup del(8p): Inverted duplication deletion of 8p [inv dup del(8p)] is a complex chromosome rearrangement leading among others to deletion of the chromosome region distal to the duplication in 8p. A new case with an inverted duplication deletion of 8p and the results of SNP-array analysis and fluorescence in situ hybridization (FISH) are reported here. Our results are in concordance with earlier reported inv dup del(8p) cases. | lld:pubmed |
pubmed-article:20162868 | pubmed:language | eng | lld:pubmed |
pubmed-article:20162868 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:20162868 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:20162868 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:20162868 | pubmed:issn | 1015-8146 | lld:pubmed |
pubmed-article:20162868 | pubmed:author | pubmed-author:GhesquiereSS | lld:pubmed |
pubmed-article:20162868 | pubmed:author | pubmed-author:DundarMM | lld:pubmed |
pubmed-article:20162868 | pubmed:author | pubmed-author:SaatciCC | lld:pubmed |
pubmed-article:20162868 | pubmed:author | pubmed-author:AlofsMM | lld:pubmed |
pubmed-article:20162868 | pubmed:author | pubmed-author:EngelenJ J... | lld:pubmed |
pubmed-article:20162868 | pubmed:author | pubmed-author:CaglayanA OAO | lld:pubmed |
pubmed-article:20162868 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:20162868 | pubmed:volume | 20 | lld:pubmed |
pubmed-article:20162868 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:20162868 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:20162868 | pubmed:pagination | 333-40 | lld:pubmed |
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pubmed-article:20162868 | pubmed:year | 2009 | lld:pubmed |
pubmed-article:20162868 | pubmed:articleTitle | Fluorescence in situ hybridization and single nucleotide polymorphism of a new case with inv dup del(8p). | lld:pubmed |
pubmed-article:20162868 | pubmed:affiliation | Kayseri Education and Research Hospital, Department of Medical Genetics, Kayseri, Turkey. okaycaglayan@yahoo.com | lld:pubmed |
pubmed-article:20162868 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:20162868 | pubmed:publicationType | Case Reports | lld:pubmed |