Assessment of association between variants and haplotypes of the remaining TBX1 gene and manifestations of congenital heart defects in 22q11.2 deletion patients. Issue 4 (1st April 2004)

Record Type:: Journal Article
Title:: Assessment of association between variants and haplotypes of the remaining TBX1 gene and manifestations of congenital heart defects in 22q11.2 deletion patients. Issue 4 (1st April 2004)
Main Title:: Assessment of association between variants and haplotypes of the remaining TBX1 gene and manifestations of congenital heart defects in 22q11.2 deletion patients
Authors:: Rauch, A
Devriendt, K
Koch, A
Rauch, R
Gewillig, M
Kraus, C
Weyand, M
Singer, H
Reis, A
Hofbeck, M
Abstract:
Is Part Of:: Journal of medical genetics. Volume 41:Issue 4(2004)
Journal:: Journal of medical genetics
Issue:: Volume 41:Issue 4(2004)
Issue Display:: Volume 41, Issue 4 (2004)
Year:: 2004
Volume:: 41
Issue:: 4
Issue Sort Value:: 2004-0041-0004-0000
Page Start:: e40
Page End:: e40
Publication Date:: 2004-04-01
Subjects:: 22q11.2 deletion -- linkage disequilibrium block structure -- TBX1 -- congenital heart defect
DGS/VCFS, DiGeorge or velocardiofacial syndrome -- GOLD, graphical package for overview of linkage disequilibrium -- LD, linkage disequilibrium -- PHASE, software package for phylogenetics and sequence evolution -- SNP, single nucleotide polymorphism
Medical genetics -- Periodicals
616.042
Journal URLs:: http://jmg.bmjjournals.com/ ↗
http://www.bmj.com/archive ↗
DOI:: 10.1136/jmg.2003.010975 ↗
Languages:: English
ISSNs:: 1468-6244
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store
Ingest File:: 17966.xml