| P2093 | author name string | P Khowsathit | |
| | A Khositseth | |
| | N Ruangdaraganon | |
| | C Tocharoentanaphol | |
| P2860 | cites work | Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11 | Q28255966 |
| | Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects | Q33595838 |
| | Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis | Q33595849 |
| | DiGeorge syndrome: part of CATCH 22. | Q33595892 |
| | Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome | Q41091241 |
| | The genetic basis of pediatric cardiovascular disease | Q41415560 |
| | Chromosomes 22q11 deletion syndrome: an update and review for the primary pediatrician | Q41471214 |
| | Congenital heart disease: prevalence at livebirth. The Baltimore-Washington Infant Study | Q46070194 |
| | Velo-cardio-facial syndrome associated with ventricular septal defect, pulmonary atresia, and hypoplastic pulmonary arteries | Q52231764 |
| | Deletion 22q11 in patients with interrupted aortic arch | Q58193949 |
| | Frequency of a 22q11 deletion in patients with conotruncal cardiac malformations: a prospective study | Q70953358 |
| | CATCHing a break on 22 | Q72048110 |
| | Truncus arteriosus communis associated with chromosome 22q11 deletion | Q73746117 |
| | Frequency of 22q11 deletions in patients with conotruncal defects | Q77107628 |
| P433 | issue | 5 | |
| P304 | page(s) | 570-573 | |
| P577 | publication date | 2005-09-01 | |
| P1433 | published in | Pediatric Cardiology | Q2232591 |
| P1476 | title | Chromosome 22q11 deletions in patients with conotruncal heart defects. | |
| P478 | volume | 26 | |