DiGeorge subtypes of nonsyndromic conotruncal defects: evidence against a major role of TBX1 Gene
- 17 April 2003
- journal article
- research article
- Published by Springer Nature in European Journal of Human Genetics
- Vol. 11 (4) , 349-351
- https://doi.org/10.1038/sj.ejhg.5200956
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathwaysHuman Molecular Genetics, 2002
- Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in miceNature, 2001
- DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1Nature Genetics, 2001
- Isolation and Characterization of a Gene from the DiGeorge Chromosomal Region Homologous to the MouseTbx1GeneGenomics, 1997
- Recurrence risk figures for isolated tetralogy of Fallot after screening for 22q11 microdeletion.Journal of Medical Genetics, 1997
- Comparison of occurrence of genetic syndromes in ventricular septal defect with pulmonic stenosis (classic tetralogy of Fallot) versus ventricular septal defect with pulmonic atresiaThe American Journal of Cardiology, 1996
- Associated cardiac anomalies in isolated and syndromic patients with tetralogy of fallotThe American Journal of Cardiology, 1996
- Tetralogy of Fallot associated with chromosome 22q11 deletionThe American Journal of Cardiology, 1995
- Routine diagnosis of DiGeorge syndrome by fluorescent in situ hybridizationHuman Genetics, 1993
- Tetralogy of Fallot in three siblings: a familial study and review of the literatureEuropean Journal of Pediatrics, 1992