Matches in DBpedia 2015-04 for { <http://dbpedia.org/resource/1q21.1_deletion_syndrome> ?p ?o }
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- 1q21.1_deletion_syndrome abstract "1q21.1 deletion syndrome or 1q21.1 (recurrent) microdeletion is a rare aberration of chromosome 1.A human cell has one pair of identical chromosomes on chromosome 1. With the 1q21.1 deletion syndrome, one chromosome of the pair is not complete, because a part of the sequence of the chromosome is missing. One chromosome has the normal length and the other is too short.In 1q21.1, the '1' stands for chromosome 1, the 'q' stands for the long arm of the chromosome and '21.1' stands for the part of the long arm in which the deletion is situated.The syndrome is a form of the 1q21.1 copy number variations and it is a deletion in the distal area of the 1q21.1 part. The CNV leads to a very variable phenotype and the manifestations in individuals are quite variable. Some people who have the syndrome can function in a normal way, while others have symptoms of mental retardation and various physical anomalies.1q21.1 microdeletion is a very rare chromosomal condition. Only 46 individuals with this deletion have been reported in the medical literature as of August 2011.".
- 1q21.1_deletion_syndrome icd10 "Q93.5".
- 1q21.1_deletion_syndrome omim "612474".
- 1q21.1_deletion_syndrome thumbnail Chromosome_1_to_1q21.1.jpg?width=300.
- 1q21.1_deletion_syndrome wikiPageExternalLink deletion1q21-1.blogspot.com.
- 1q21.1_deletion_syndrome wikiPageExternalLink jgregorysharingsstories.blogspot.com.
- 1q21.1_deletion_syndrome wikiPageExternalLink www.1q21-1microdeletionsyndrome.weebly.com.
- 1q21.1_deletion_syndrome wikiPageExternalLink 144.
- 1q21.1_deletion_syndrome wikiPageExternalLink NBK52787.
- 1q21.1_deletion_syndrome wikiPageExternalLink cite&retmode=ref&cmd=prlinks&id=19955444.
- 1q21.1_deletion_syndrome wikiPageExternalLink OC_Exp.php?lng=EN&Expert=250989.
- 1q21.1_deletion_syndrome wikiPageID "28395600".
- 1q21.1_deletion_syndrome wikiPageRevisionID "642250428".
- 1q21.1_deletion_syndrome hasPhotoCollection 1q21.1_deletion_syndrome.
- 1q21.1_deletion_syndrome icd "Q93.5".
- 1q21.1_deletion_syndrome medlineplus "1".
- 1q21.1_deletion_syndrome name "1".
- 1q21.1_deletion_syndrome omim "612474".
- 1q21.1_deletion_syndrome subject Category:Autosomal_monosomies_and_deletions.
- 1q21.1_deletion_syndrome subject Category:Congenital_disorders.
- 1q21.1_deletion_syndrome subject Category:Developmental_biology.
- 1q21.1_deletion_syndrome subject Category:Hematology.
- 1q21.1_deletion_syndrome subject Category:Syndromes.
- 1q21.1_deletion_syndrome type Disease.
- 1q21.1_deletion_syndrome type Medicine.
- 1q21.1_deletion_syndrome type Thing.
- 1q21.1_deletion_syndrome type Q12136.
- 1q21.1_deletion_syndrome comment "1q21.1 deletion syndrome or 1q21.1 (recurrent) microdeletion is a rare aberration of chromosome 1.A human cell has one pair of identical chromosomes on chromosome 1. With the 1q21.1 deletion syndrome, one chromosome of the pair is not complete, because a part of the sequence of the chromosome is missing.".
- 1q21.1_deletion_syndrome label "1q21.1 deletion syndrome".
- 1q21.1_deletion_syndrome label "1q21.1-Deletionssyndrom".
- 1q21.1_deletion_syndrome label "1q21.1-deletiesyndroom".
- 1q21.1_deletion_syndrome sameAs 1q21.1-Deletionssyndrom.
- 1q21.1_deletion_syndrome sameAs 1q21.1-deletiesyndroom.
- 1q21.1_deletion_syndrome sameAs m.0crhxnt.
- 1q21.1_deletion_syndrome sameAs Q209049.
- 1q21.1_deletion_syndrome sameAs Q209049.
- 1q21.1_deletion_syndrome wasDerivedFrom 1q21.1_deletion_syndrome?oldid=642250428.
- 1q21.1_deletion_syndrome depiction Chromosome_1_to_1q21.1.jpg.
- 1q21.1_deletion_syndrome isPrimaryTopicOf 1q21.1_deletion_syndrome.
- 1q21.1_deletion_syndrome name "1q21.1 deletion syndrome".