CZ:Ref:DOI:10.1038/ng.454: Difference between revisions

From Citizendium
Jump to navigation Jump to search
imported>Daniel Mietchen
(started)
 
imported>Daniel Mietchen
(slight rephrasing)
 
Line 1: Line 1:
{{cite journal| author=Yang XR, Ng D, Alcorta DA, Liebsch NJ, Sheridan E, Li S et al.| title=T (brachyury) gene duplication confers major susceptibility to familial chordoma | journal=Nat Genet | year= 2009 | volume= 41 | issue= 11 | pages= 1176-8 | pmid=19801981  
{{cite journal| author=Yang XR, Ng D, Alcorta DA, Liebsch NJ, Sheridan E, Li S et al.| title=T (brachyury) gene duplication confers major susceptibility to familial chordoma | journal=Nat Genet | year= 2009 | volume= 41 | issue= 11 | pages= 1176-8 | pmid=19801981  
| url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=clinical.uthscsa.edu/cite&retmode=ref&cmd=prlinks&id=19801981 | doi=10.1038/ng.454 }}
| url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=clinical.uthscsa.edu/cite&retmode=ref&cmd=prlinks&id=19801981 | doi=10.1038/ng.454 }}
:Based on [[comparative genomic hybridization]] data from families with [[chordoma]] patients, variations in the [[chromosome band|6q27]] region of the [[human chromosome 6]] were found to be correlated with the disease, thus suggesting the [[T (gene)|T]] [[gene]] as a potential [[susceptibility gene]] for this severe condition.
:Based on [[comparative genomic hybridization]] data from four affected families, variations in the [[chromosome band|6q27]] region of the [[human chromosome 6]] were found to be correlated with [[chordoma]], thus suggesting the [[T (gene)|T]] [[gene]] as a potential [[susceptibility gene]] for the disease.

Latest revision as of 16:48, 11 May 2010

Yang XR, Ng D, Alcorta DA, Liebsch NJ, Sheridan E, Li S et al. (2009). "T (brachyury) gene duplication confers major susceptibility to familial chordoma". Nat Genet 41 (11): 1176-8. DOI:10.1038/ng.454. PMID 19801981. Research Blogging[e]

Based on comparative genomic hybridization data from four affected families, variations in the 6q27 region of the human chromosome 6 were found to be correlated with chordoma, thus suggesting the T gene as a potential susceptibility gene for the disease.