Matches in DBpedia 2016-04 for { <http://dbpedia.org/resource/17q21.31_microdeletion_syndrome> ?p ?o }
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- 17q21.31_microdeletion_syndrome abstract "17q21.31 microdeletion syndrome (Koolen De Vries syndrome) is a rare genetic disorder caused by a deletion of a segment of chromosome 17 which contains six genes. This deletion syndrome was discovered independently in 2006 by three different research groups.".
- 17q21.31_microdeletion_syndrome omim "610443".
- 17q21.31_microdeletion_syndrome wikiPageExternalLink www.17q21.com.
- 17q21.31_microdeletion_syndrome wikiPageExternalLink cite&retmode=ref&cmd=prlinks&id=19447831.
- 17q21.31_microdeletion_syndrome wikiPageExternalLink cite&retmode=ref&cmd=prlinks&id=20110647.
- 17q21.31_microdeletion_syndrome wikiPageExternalLink cite&retmode=ref&cmd=prlinks&id=20606400.
- 17q21.31_microdeletion_syndrome wikiPageExternalLink OC_Exp.php?lng=EN&Expert=96169.
- 17q21.31_microdeletion_syndrome wikiPageExternalLink 17q21.31%20microdeletions%20FTNW.pdf.
- 17q21.31_microdeletion_syndrome wikiPageID "27588735".
- 17q21.31_microdeletion_syndrome wikiPageLength "9826".
- 17q21.31_microdeletion_syndrome wikiPageOutDegree "22".
- 17q21.31_microdeletion_syndrome wikiPageRevisionID "695597528".
- 17q21.31_microdeletion_syndrome wikiPageWikiLink Atrial_septal_defect.
- 17q21.31_microdeletion_syndrome wikiPageWikiLink Base_pair.
- 17q21.31_microdeletion_syndrome wikiPageWikiLink C17orf69.
- 17q21.31_microdeletion_syndrome wikiPageWikiLink Category:Autosomal_monosomies_and_deletions.
- 17q21.31_microdeletion_syndrome wikiPageWikiLink Chromosome_17_(human).
- 17q21.31_microdeletion_syndrome wikiPageWikiLink Corticotropin-releasing_hormone_receptor_1.
- 17q21.31_microdeletion_syndrome wikiPageWikiLink Deletion_(genetics).
- 17q21.31_microdeletion_syndrome wikiPageWikiLink Depigmentation.
- 17q21.31_microdeletion_syndrome wikiPageWikiLink Developmental_coordination_disorder.
- 17q21.31_microdeletion_syndrome wikiPageWikiLink Epilepsy.
- 17q21.31_microdeletion_syndrome wikiPageWikiLink Gene_duplication.
- 17q21.31_microdeletion_syndrome wikiPageWikiLink Genetic_disorder.
- 17q21.31_microdeletion_syndrome wikiPageWikiLink Hypotonia.
- 17q21.31_microdeletion_syndrome wikiPageWikiLink KIAA1267.
- 17q21.31_microdeletion_syndrome wikiPageWikiLink Low_copy_repeats.
- 17q21.31_microdeletion_syndrome wikiPageWikiLink Microdeletion_syndrome.
- 17q21.31_microdeletion_syndrome wikiPageWikiLink Non-allelic_homologous_recombination.
- 17q21.31_microdeletion_syndrome wikiPageWikiLink Orphanet.
- 17q21.31_microdeletion_syndrome wikiPageWikiLink Polymorphism_(biology).
- 17q21.31_microdeletion_syndrome wikiPageWikiLink Tau_protein.
- 17q21.31_microdeletion_syndrome wikiPageWikiLink Ventricular_septal_defect.
- 17q21.31_microdeletion_syndrome wikiPageWikiLinkText "17q21.31 microdeletion syndrome".
- 17q21.31_microdeletion_syndrome genereviewsname "17".
- 17q21.31_microdeletion_syndrome genereviewsnbk "NBK24676".
- 17q21.31_microdeletion_syndrome name "17".
- 17q21.31_microdeletion_syndrome omim "610443".
- 17q21.31_microdeletion_syndrome wikiPageUsesTemplate Template:Chromosomal_abnormalities.
- 17q21.31_microdeletion_syndrome wikiPageUsesTemplate Template:Cite_journal.
- 17q21.31_microdeletion_syndrome wikiPageUsesTemplate Template:DECIPHER.
- 17q21.31_microdeletion_syndrome wikiPageUsesTemplate Template:Infobox_disease.
- 17q21.31_microdeletion_syndrome wikiPageUsesTemplate Template:Mutation.
- 17q21.31_microdeletion_syndrome wikiPageUsesTemplate Template:Refbegin.
- 17q21.31_microdeletion_syndrome wikiPageUsesTemplate Template:Refend.
- 17q21.31_microdeletion_syndrome wikiPageUsesTemplate Template:Reflist.
- 17q21.31_microdeletion_syndrome wikiPageUsesTemplate Template:Research_help.
- 17q21.31_microdeletion_syndrome subject Category:Autosomal_monosomies_and_deletions.
- 17q21.31_microdeletion_syndrome hypernym Disorder.
- 17q21.31_microdeletion_syndrome type Disease.
- 17q21.31_microdeletion_syndrome type Redirect.
- 17q21.31_microdeletion_syndrome type Thing.
- 17q21.31_microdeletion_syndrome type Q12136.
- 17q21.31_microdeletion_syndrome comment "17q21.31 microdeletion syndrome (Koolen De Vries syndrome) is a rare genetic disorder caused by a deletion of a segment of chromosome 17 which contains six genes. This deletion syndrome was discovered independently in 2006 by three different research groups.".
- 17q21.31_microdeletion_syndrome label "17q21.31 microdeletion syndrome".
- 17q21.31_microdeletion_syndrome sameAs Q4553565.
- 17q21.31_microdeletion_syndrome sameAs m.0c4263m.
- 17q21.31_microdeletion_syndrome sameAs Q4553565.
- 17q21.31_microdeletion_syndrome wasDerivedFrom 17q21.31_microdeletion_syndrome?oldid=695597528.
- 17q21.31_microdeletion_syndrome isPrimaryTopicOf 17q21.31_microdeletion_syndrome.
- 17q21.31_microdeletion_syndrome name "17q21.31 microdeletion syndrome (Koolen De Vries Syndrome)".