Matches in DBpedia 2016-04 for { <http://wikidata.dbpedia.org/resource/Q5369177> ?p ?o }
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- Q5369177 subject Q7022922.
- Q5369177 subject Q7031586.
- Q5369177 subject Q8280464.
- Q5369177 abstract "Derivative 22 syndrome, or der(22), is a rare disorder associated with multiple congenital anomalies, including profound mental retardation, preauricular skin tags or pits, and conotruncal heart defects. It can occur in offspring of carriers of the constitutional chromosomal translocation t(11;22)(q23;q11), owing to a 3:1 meiotic malsegregation event resulting in partial trisomy of chromosomes 11 and 22. An unbalanced translocation between chromosomes 11 & 22 is described as Emanuel syndrome. It was characterized in 1980.".
- Q5369177 omim "609029".
- Q5369177 wikiPageExternalLink 11.
- Q5369177 wikiPageExternalLink Emanuel_syndrome.aspx.
- Q5369177 wikiPageExternalLink es1.htm.
- Q5369177 wikiPageExternalLink research.htm.
- Q5369177 wikiPageExternalLink emanuel-syndrome-0.
- Q5369177 wikiPageExternalLink symptoms.htm.
- Q5369177 wikiPageWikiLink Q1100988.
- Q5369177 wikiPageWikiLink Q1497481.
- Q5369177 wikiPageWikiLink Q162925.
- Q5369177 wikiPageWikiLink Q1753547.
- Q5369177 wikiPageWikiLink Q183560.
- Q5369177 wikiPageWikiLink Q222634.
- Q5369177 wikiPageWikiLink Q3179593.
- Q5369177 wikiPageWikiLink Q37748.
- Q5369177 wikiPageWikiLink Q431643.
- Q5369177 wikiPageWikiLink Q7022922.
- Q5369177 wikiPageWikiLink Q7031586.
- Q5369177 wikiPageWikiLink Q727096.
- Q5369177 wikiPageWikiLink Q753805.
- Q5369177 wikiPageWikiLink Q8280464.
- Q5369177 wikiPageWikiLink Q844903.
- Q5369177 wikiPageWikiLink Q847096.
- Q5369177 wikiPageWikiLink Q916504.
- Q5369177 name "Emanuel syndrome".
- Q5369177 omim "609029".
- Q5369177 type Disease.
- Q5369177 type Thing.
- Q5369177 type Q12136.
- Q5369177 comment "Derivative 22 syndrome, or der(22), is a rare disorder associated with multiple congenital anomalies, including profound mental retardation, preauricular skin tags or pits, and conotruncal heart defects. It can occur in offspring of carriers of the constitutional chromosomal translocation t(11;22)(q23;q11), owing to a 3:1 meiotic malsegregation event resulting in partial trisomy of chromosomes 11 and 22. An unbalanced translocation between chromosomes 11 & 22 is described as Emanuel syndrome.".
- Q5369177 label "Emanuel syndrome".
- Q5369177 name "Emanuel syndrome".