Matches in DBpedia 2015-10 for { <http://dbpedia.org/resource/Chromosome_15q_partial_deletion> ?p ?o }
Showing triples 1 to 34 of
34
with 100 triples per page.
- Chromosome_15q_partial_deletion abstract "Chromosome 15q partial deletion is an extremely rare human genetic disorder, caused by a chromosomal aberration in which the long ("q") arm of one copy of chromosome 15 is deleted, or partially deleted. If the mother's copy of the chromosomal arm is deleted, Angelman syndrome results. If the father's copy of the chromosomal arm is deleted, Prader-Willi syndrome results. The smallest observed region that can result in these syndromes when deleted is therefore called the PWS/AS critical region and is situated at 15q11-q13. In addition to deletions, uniparental disomy of chromosome 15 gives rise to the same genetic disorders, indicating that genomic imprinting must occur in this region.".
- Chromosome_15q_partial_deletion wikiPageID "88863".
- Chromosome_15q_partial_deletion wikiPageLength "1027".
- Chromosome_15q_partial_deletion wikiPageOutDegree "12".
- Chromosome_15q_partial_deletion wikiPageRevisionID "558449444".
- Chromosome_15q_partial_deletion wikiPageWikiLink Angelman_syndrome.
- Chromosome_15q_partial_deletion wikiPageWikiLink Category:Genetic_disorders_with_no_OMIM.
- Chromosome_15q_partial_deletion wikiPageWikiLink Chromosome.
- Chromosome_15q_partial_deletion wikiPageWikiLink Chromosome_15q_trisomy.
- Chromosome_15q_partial_deletion wikiPageWikiLink Deletion_(genetics).
- Chromosome_15q_partial_deletion wikiPageWikiLink Genetic_deletion.
- Chromosome_15q_partial_deletion wikiPageWikiLink Genetic_disorder.
- Chromosome_15q_partial_deletion wikiPageWikiLink Genetics.
- Chromosome_15q_partial_deletion wikiPageWikiLink Genomic_imprinting.
- Chromosome_15q_partial_deletion wikiPageWikiLink Human.
- Chromosome_15q_partial_deletion wikiPageWikiLink Prader-Willi_syndrome.
- Chromosome_15q_partial_deletion wikiPageWikiLink Prader–Willi_syndrome.
- Chromosome_15q_partial_deletion wikiPageWikiLink Uniparental_disomy.
- Chromosome_15q_partial_deletion wikiPageWikiLinkText "Chromosome 15q partial deletion".
- Chromosome_15q_partial_deletion wikiPageWikiLinkText "chromosome 15q partial deletion".
- Chromosome_15q_partial_deletion hasPhotoCollection Chromosome_15q_partial_deletion.
- Chromosome_15q_partial_deletion wikiPageUsesTemplate Template:Genetic-disorder-stub.
- Chromosome_15q_partial_deletion wikiPageUsesTemplate Template:Unreferenced.
- Chromosome_15q_partial_deletion subject Category:Genetic_disorders_with_no_OMIM.
- Chromosome_15q_partial_deletion type Article.
- Chromosome_15q_partial_deletion type Article.
- Chromosome_15q_partial_deletion type Disorder.
- Chromosome_15q_partial_deletion comment "Chromosome 15q partial deletion is an extremely rare human genetic disorder, caused by a chromosomal aberration in which the long ("q") arm of one copy of chromosome 15 is deleted, or partially deleted. If the mother's copy of the chromosomal arm is deleted, Angelman syndrome results. If the father's copy of the chromosomal arm is deleted, Prader-Willi syndrome results.".
- Chromosome_15q_partial_deletion label "Chromosome 15q partial deletion".
- Chromosome_15q_partial_deletion sameAs m.0m72k.
- Chromosome_15q_partial_deletion sameAs Q5113911.
- Chromosome_15q_partial_deletion sameAs Q5113911.
- Chromosome_15q_partial_deletion wasDerivedFrom Chromosome_15q_partial_deletion?oldid=558449444.
- Chromosome_15q_partial_deletion isPrimaryTopicOf Chromosome_15q_partial_deletion.