Chromosome 10p13-14 and 22q11 deletion screening in 100 patients with isolated and syndromic conotruncal heart defects. Issue 4 (1st April 2002)

Record Type:: Journal Article
Title:: Chromosome 10p13-14 and 22q11 deletion screening in 100 patients with isolated and syndromic conotruncal heart defects. Issue 4 (1st April 2002)
Main Title:: Chromosome 10p13-14 and 22q11 deletion screening in 100 patients with isolated and syndromic conotruncal heart defects
Authors:: Voigt, R
Maier-Weidmann, M
Lange, P E
Haaf, T
Abstract:
Is Part Of:: Journal of medical genetics. Volume 39:Issue 4(2002)
Journal:: Journal of medical genetics
Issue:: Volume 39:Issue 4(2002)
Issue Display:: Volume 39, Issue 4 (2002)
Year:: 2002
Volume:: 39
Issue:: 4
Issue Sort Value:: 2002-0039-0004-0000
Page Start:: e16
Page End:: e16
Publication Date:: 2002-04-01
Subjects:: conotruncal heart defects -- 22q11 deletion -- 10p13-14 deletion
CTHD, conotruncal heart defects -- VCFS, velocardiofacial syndrome -- DGS, DiGeorge syndrome -- CTAFS, conotruncal anomaly-face syndrome -- TOF, tetralogy of Fallot
Medical genetics -- Periodicals
616.042
Journal URLs:: http://jmg.bmjjournals.com/ ↗
http://www.bmj.com/archive ↗
DOI:: 10.1136/jmg.39.4.e16 ↗
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:: 18222.xml