Matches in DBpedia 2016-04 for { ?s ?p "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."@en }
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- 2p15-16.1_microdeletion_syndrome 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 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.".
- 2p15-16.1_microdeletion_syndrome 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 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.".