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- Q4633988 subject Q8280463.
- Q4633988 abstract "2p15-16.1 microdeletion is a rare genetic disorder caused by a small deletion in the short arm of human chromosome 2. First described in two patients in 2007, by 2013 only 21 (missing reference for the other ~17 patients) people have been reported as having the disorder in the medical literature.".
- Q4633988 thumbnail Chromosome_2.svg?width=300.
- Q4633988 wikiPageExternalLink OC_Exp.php?lng=EN&Expert=261349.
- Q4633988 wikiPageExternalLink 2p15p16.1%20microdeletions%20FTNW.pdf.
- Q4633988 wikiPageWikiLink Q106227.
- Q4633988 wikiPageWikiLink Q1316942.
- Q4633988 wikiPageWikiLink Q145911.
- Q4633988 wikiPageWikiLink Q1503008.
- Q4633988 wikiPageWikiLink Q1515833.
- Q4633988 wikiPageWikiLink Q152092.
- Q4633988 wikiPageWikiLink Q1524166.
- Q4633988 wikiPageWikiLink Q179630.
- Q4633988 wikiPageWikiLink Q18030467.
- Q4633988 wikiPageWikiLink Q18031085.
- Q4633988 wikiPageWikiLink Q18032337.
- Q4633988 wikiPageWikiLink Q18032393.
- Q4633988 wikiPageWikiLink Q18034629.
- Q4633988 wikiPageWikiLink Q18040602.
- Q4633988 wikiPageWikiLink Q18041564.
- Q4633988 wikiPageWikiLink Q18045798.
- Q4633988 wikiPageWikiLink Q18047651.
- Q4633988 wikiPageWikiLink Q183560.
- Q4633988 wikiPageWikiLink Q200779.
- Q4633988 wikiPageWikiLink Q277338.
- Q4633988 wikiPageWikiLink Q431643.
- Q4633988 wikiPageWikiLink Q4651785.
- Q4633988 wikiPageWikiLink Q488415.
- Q4633988 wikiPageWikiLink Q614013.
- Q4633988 wikiPageWikiLink Q622427.
- Q4633988 wikiPageWikiLink Q638893.
- Q4633988 wikiPageWikiLink Q6806558.
- Q4633988 wikiPageWikiLink Q6966563.
- Q4633988 wikiPageWikiLink Q7098797.
- Q4633988 wikiPageWikiLink Q7128693.
- Q4633988 wikiPageWikiLink Q7187.
- Q4633988 wikiPageWikiLink Q730877.
- Q4633988 wikiPageWikiLink Q755077.
- Q4633988 wikiPageWikiLink Q8280463.
- Q4633988 comment "2p15-16.1 microdeletion is a rare genetic disorder caused by a small deletion in the short arm of human chromosome 2. First described in two patients in 2007, by 2013 only 21 (missing reference for the other ~17 patients) people have been reported as having the disorder in the medical literature.".
- Q4633988 label "2p15-16.1 microdeletion syndrome".
- Q4633988 depiction Chromosome_2.svg.