| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1004295145 |
| P356 | DOI | 10.1097/00125817-200101000-00010 |
| P698 | PubMed publication ID | 11339377 |
| P2093 | author name string | B Dallapiccola | |
| B Marino | |||
| A Toscano | |||
| A Giannotti | |||
| M C Digilio | |||
| A Angioni | |||
| C Feltri | |||
| M A de Ioris | |||
| S Anaclerio | |||
| P2860 | cites work | Chromosome 22q11 microdeletion and isolated conotruncal heart defects | Q28764522 |
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| A genetic etiology for interruption of the aortic arch type B | Q73670410 | ||
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| 22q11.2 deletions in a series of patients with non-selective congenital heart defects: incidence, type of defects and parental origin | Q74460164 | ||
| Holt-Oram syndrome and multiple ventricular septal defects: an association suggesting a possible genetic marker? | Q74813406 | ||
| Frequency of 22q11 deletions in patients with conotruncal defects | Q77107628 | ||
| Incidence and significance of 22q11.2 hemizygosity in patients with interrupted aortic arch | Q77134630 | ||
| Prenatal detection of a tetralogy of Fallot with origin of the left pulmonary artery from the ascending aorta in a familial 22q11 microdeletion | Q77346146 | ||
| Severe truncal valve dysplasia: association with DiGeorge syndrome? | Q77399318 | ||
| P433 | issue | 1 | |
| P304 | page(s) | 45-48 | |
| P577 | publication date | 2001-01-01 | |
| P1433 | published in | Genetics in Medicine | Q15765508 |
| P1476 | title | Anatomic patterns of conotruncal defects associated with deletion 22q11 | |
| P478 | volume | 3 |
| Q37179567 | A review of the surgical management of right-sided aortic arch aneurysms |
| Q36497115 | A variant in the carboxyl-terminus of connexin 40 alters GAP junctions and increases risk for tetralogy of Fallot |
| Q43900237 | Aberrant subclavian artery origin in tetralogy of Fallot with pulmonary stenosis is associated with chromosomal or genetic abnormality |
| Q37164120 | Adults with genetic syndromes and cardiovascular abnormalities: clinical history and management |
| Q91684123 | Assessment of airway abnormalities in patients with tetralogy of Fallot, pulmonary atresia, and major aortopulmonary collaterals |
| Q58193256 | Association of DiGeorge anomaly and caudal dysplasia sequence in a neonate born to a diabetic mother |
| Q37802024 | Can clinical assessment detect 22q11.2 deletions in patients with cardiac malformations? A review |
| Q37219665 | Cardiac defects and results of cardiac surgery in 22q11.2 deletion syndrome |
| Q73882302 | Chromosome 22q11 deletion in patients with truncus arteriosus |
| Q58141926 | Chromosome 22q11.2 microdeletion in children with conotruncal heart defects: frequency, associated cardiovascular anomalies, and outcome following cardiac surgery |
| Q35182065 | Cleft palate, retrognathia and congenital heart disease in velo-cardio-facial syndrome: a phenotype correlation study |
| Q39654228 | Clinical manifestations of Deletion 22q11.2 syndrome (DiGeorge/Velo-Cardio-Facial syndrome) |
| Q35581824 | Common arterial trunk in the fetus: characteristics, associations, and outcome in a multicentre series of 23 cases. |
| Q35281043 | Complex congenital heart disease in unaffected relatives of adults with 22q11.2 deletion syndrome |
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| Q58193810 | DiGeorge subtypes of nonsyndromic conotruncal defects: evidence against a major role of TBX1 Gene |
| Q35115372 | Extracardiac features predicting 22q11.2 deletion syndrome in adult congenital heart disease |
| Q90669133 | Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association |
| Q58749774 | Genetic Imbalances in Argentinean Patients with Congenital Conotruncal Heart Defects |
| Q53465565 | Genetic counseling for the 22q11.2 deletion. |
| Q55425712 | Genetic dosage compensation in a family with velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome. |
| Q38195246 | ICON: the early diagnosis of congenital immunodeficiencies |
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| Q55410868 | Some Isolated Cardiac Malformations Can Be Related to Laterality Defects. |
| Q73565436 | Tetralogy of Fallot with aortic valvular stenosis and deletion 22q11 |
| Q81376555 | The fate of children with microdeletion 22q11.2 syndrome and congenital heart defect: clinical course and cardiac outcome |
| Q51923078 | Three patients with oculo-auriculo-vertebral spectrum and microdeletion 22q11.2. |
| Q26866024 | Transposition of great arteries: new insights into the pathogenesis |
| Q58193870 | Ventricular septal defect and deletion of chromosome 22q11: anatomical types and aortic arch anomalies |
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