Matches in DBpedia 2016-04 for { <http://dbpedia.org/resource/2p15-16.1_microdeletion_syndrome> ?p ?o }
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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.".
- 2p15-16.1_microdeletion_syndrome thumbnail Chromosome_2.svg?width=300.
- 2p15-16.1_microdeletion_syndrome wikiPageExternalLink OC_Exp.php?lng=EN&Expert=261349.
- 2p15-16.1_microdeletion_syndrome wikiPageExternalLink 2p15p16.1%20microdeletions%20FTNW.pdf.
- 2p15-16.1_microdeletion_syndrome wikiPageID "17350393".
- 2p15-16.1_microdeletion_syndrome wikiPageLength "5902".
- 2p15-16.1_microdeletion_syndrome wikiPageOutDegree "41".
- 2p15-16.1_microdeletion_syndrome wikiPageRevisionID "658864565".
- 2p15-16.1_microdeletion_syndrome wikiPageWikiLink AHSA2.
- 2p15-16.1_microdeletion_syndrome wikiPageWikiLink Anatomical_terms_of_location.
- 2p15-16.1_microdeletion_syndrome wikiPageWikiLink BCL11A.
- 2p15-16.1_microdeletion_syndrome wikiPageWikiLink Base_pair.
- 2p15-16.1_microdeletion_syndrome wikiPageWikiLink C2orf74.
- 2p15-16.1_microdeletion_syndrome wikiPageWikiLink Camptodactyly.
- 2p15-16.1_microdeletion_syndrome wikiPageWikiLink Category:Autosomal_monosomies_and_deletions.
- 2p15-16.1_microdeletion_syndrome wikiPageWikiLink Chromosome_2_(human).
- 2p15-16.1_microdeletion_syndrome wikiPageWikiLink Cortical_dysplasia.
- 2p15-16.1_microdeletion_syndrome wikiPageWikiLink FANCL.
- 2p15-16.1_microdeletion_syndrome wikiPageWikiLink Gene.
- 2p15-16.1_microdeletion_syndrome wikiPageWikiLink Genetic_disorder.
- 2p15-16.1_microdeletion_syndrome wikiPageWikiLink Hydronephrosis.
- 2p15-16.1_microdeletion_syndrome wikiPageWikiLink Intellectual_disability.
- 2p15-16.1_microdeletion_syndrome wikiPageWikiLink KIAA1841.
- 2p15-16.1_microdeletion_syndrome wikiPageWikiLink Locus_(genetics).
- 2p15-16.1_microdeletion_syndrome wikiPageWikiLink Medical_literature.
- 2p15-16.1_microdeletion_syndrome wikiPageWikiLink Microcephaly.
- 2p15-16.1_microdeletion_syndrome wikiPageWikiLink Mosaic_(genetics).
- 2p15-16.1_microdeletion_syndrome wikiPageWikiLink Nasal_bridge.
- 2p15-16.1_microdeletion_syndrome wikiPageWikiLink Optic_nerve_hypoplasia.
- 2p15-16.1_microdeletion_syndrome wikiPageWikiLink Orphanet.
- 2p15-16.1_microdeletion_syndrome wikiPageWikiLink PAPOLG.
- 2p15-16.1_microdeletion_syndrome wikiPageWikiLink PEX13.
- 2p15-16.1_microdeletion_syndrome wikiPageWikiLink PUS10.
- 2p15-16.1_microdeletion_syndrome wikiPageWikiLink Palpebral_fissure.
- 2p15-16.1_microdeletion_syndrome wikiPageWikiLink Philtrum.
- 2p15-16.1_microdeletion_syndrome wikiPageWikiLink Pigeon_toe.
- 2p15-16.1_microdeletion_syndrome wikiPageWikiLink Pseudogene.
- 2p15-16.1_microdeletion_syndrome wikiPageWikiLink Ptosis_(eyelid).
- 2p15-16.1_microdeletion_syndrome wikiPageWikiLink REL.
- 2p15-16.1_microdeletion_syndrome wikiPageWikiLink SNORA70B.
- 2p15-16.1_microdeletion_syndrome wikiPageWikiLink Syndrome.
- 2p15-16.1_microdeletion_syndrome wikiPageWikiLink Telecanthus.
- 2p15-16.1_microdeletion_syndrome wikiPageWikiLink USP34.
- 2p15-16.1_microdeletion_syndrome wikiPageWikiLink VRK2.
- 2p15-16.1_microdeletion_syndrome wikiPageWikiLink Wikt:de_novo.
- 2p15-16.1_microdeletion_syndrome wikiPageWikiLink XPO1.
- 2p15-16.1_microdeletion_syndrome wikiPageWikiLink File:Chromosome_2.svg.
- 2p15-16.1_microdeletion_syndrome wikiPageWikiLinkText "2p15-16.1 microdeletion syndrome".
- 2p15-16.1_microdeletion_syndrome wikiPageUsesTemplate Template:Chromosomal_abnormalities.
- 2p15-16.1_microdeletion_syndrome wikiPageUsesTemplate Template:DECIPHER.
- 2p15-16.1_microdeletion_syndrome wikiPageUsesTemplate Template:OMIM.
- 2p15-16.1_microdeletion_syndrome wikiPageUsesTemplate Template:Reflist.
- 2p15-16.1_microdeletion_syndrome subject Category:Autosomal_monosomies_and_deletions.
- 2p15-16.1_microdeletion_syndrome hypernym Disorder.
- 2p15-16.1_microdeletion_syndrome type Disease.
- 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.".
- 2p15-16.1_microdeletion_syndrome label "2p15-16.1 microdeletion syndrome".
- 2p15-16.1_microdeletion_syndrome sameAs Q4633988.
- 2p15-16.1_microdeletion_syndrome sameAs m.043mgpp.
- 2p15-16.1_microdeletion_syndrome sameAs Q4633988.
- 2p15-16.1_microdeletion_syndrome wasDerivedFrom 2p15-16.1_microdeletion_syndrome?oldid=658864565.
- 2p15-16.1_microdeletion_syndrome depiction Chromosome_2.svg.
- 2p15-16.1_microdeletion_syndrome isPrimaryTopicOf 2p15-16.1_microdeletion_syndrome.