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Statements

Subject Item
dbr:Ring_chromosome_18
rdf:type
owl:Thing wikidata:Q12136 dbo:Disease
rdfs:label
Zespół pierścieniowego chromosomu 18 Ring chromosome 18 Ring 18
rdfs:comment
La Ring 18 è una malattia genetica causata dalla cancellazione delle due punte del cromosoma 18 che comporta la formazione di un cromosoma a forma d'anello. È stato descritto la prima volta nel 1964. Zespół pierścieniowego chromosomu 18 (ang. Ring chromosome 18 syndrome, r(18) syndrome) – zespół wad wrodzonych spowodowany obecnością we wszystkich komórkach somatycznych organizmu (lub ich części - mozaicyzm) chromosomu pierścieniowego z utratą fragmentów chromosomów 18p i 18q. Ring chromosome 18 is a genetic condition caused by a deletion of the two ends of chromosome 18 followed by the formation of a ring-shaped chromosome. It was first reported in 1964.
foaf:name
Ring chromosome 18
dbp:name
Ring chromosome 18
foaf:depiction
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medical genetics
dbp:synonyms
Ring chromosome 18
dbo:abstract
Zespół pierścieniowego chromosomu 18 (ang. Ring chromosome 18 syndrome, r(18) syndrome) – zespół wad wrodzonych spowodowany obecnością we wszystkich komórkach somatycznych organizmu (lub ich części - mozaicyzm) chromosomu pierścieniowego z utratą fragmentów chromosomów 18p i 18q. La Ring 18 è una malattia genetica causata dalla cancellazione delle due punte del cromosoma 18 che comporta la formazione di un cromosoma a forma d'anello. È stato descritto la prima volta nel 1964. Ring chromosome 18 is a genetic condition caused by a deletion of the two ends of chromosome 18 followed by the formation of a ring-shaped chromosome. It was first reported in 1964.
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538304.0
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wikipedia-en:Ring_chromosome_18