Association of chromosome 22q11 deletion with isolated anomalies of aortic arch laterality and branching
Top Cited Papers
- 1 June 2001
- journal article
- Published by Elsevier
- Vol. 37 (8) , 2114-2119
- https://doi.org/10.1016/s0735-1097(01)01286-4
Abstract
No abstract availableKeywords
This publication has 22 references indexed in Scilit:
- Congenital heart disease in mice deficient for the DiGeorge syndrome regionNature, 1999
- Molecular Definition of 22q11 Deletions in 151 Velo-Cardio-Facial Syndrome PatientsAmerican Journal of Human Genetics, 1997
- The 22q11.2 Deletion: Screening, Diagnostic Workup, and Outcome of Results; Report on 181 PatientsGenetic Testing, 1997
- Search for 22q11 deletion in non-syndromic conotruncal cardiac defectsEuropean Journal of Pediatrics, 1996
- Tetralogy of fallot with pulmonary atresia associated with chromosome 22q11 deletionJournal of the American College of Cardiology, 1996
- Covert congenital cardiovascular malformations discovered in an autopsy series of nearly 5,000 casesCardiovascular Pathology, 1996
- Chromosome 22q11 microdeletions in tetralogy of Fallot.Archives of Disease in Childhood, 1996
- Tetralogy of Fallot associated with chromosome 22q11 deletionThe American Journal of Cardiology, 1995
- 22q11 deletions in isolated and syndromic patients with tetralogy of FallotHuman Genetics, 1995
- Cardiac neural crest contribution to the pulmonary artery and sixth aortic arch artery complex in chick embryos aged 6 to 18 daysThe Anatomical Record, 1993