| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S0735-1097(97)00240-4 |
| P698 | PubMed publication ID | 9316541 |
| P2093 | author name string | R Matsuoka | |
| M Ando | |||
| K Momma | |||
| P2860 | cites work | The anatomy of common aorticopulmonary trunk (truncus arteriosus communis) and its embryologic implications. A study of 57 necropsy cases | Q28256568 |
| Role of neural crest in congenital heart disease | Q37942184 | ||
| Velo-cardio-facial syndrome. Intrafamilial variability of the phenotype | Q40779186 | ||
| “Agenesis” of ductus arteriosus associated with the syndrome of tetralogy of fallot and absent pulmonary valve | Q43924018 | ||
| Confirmation that the conotruncal anomaly face syndrome is associated with a deletion within 22q11.2. | Q52212966 | ||
| Cardiovascular anomalies in DiGeorge syndrome and importance of neural crest as a possible pathogenetic factor. | Q52261048 | ||
| Truncus arteriosus communis. Clinical, angiocardiographic, and pathologic findings in 100 patients | Q67851396 | ||
| Fetal cardiac morphology of tetralogy of Fallot with absent pulmonary valve in the rat | Q68920990 | ||
| Pathogenesis of persistent truncus arteriosus and dextroposed aorta in the chick embryo after neural crest ablation | Q69688201 | ||
| Alteration of early vascular development after ablation of cranial neural crest | Q69802267 | ||
| Tetralogy of Fallot with pulmonary atresia associated with chromosome 22q11 deletion | Q70790012 | ||
| Dependence of thymus development on derivatives of the neural crest | Q70999774 | ||
| Tetralogy of Fallot associated with chromosome 22q11 deletion | Q72064736 | ||
| Deletion within chromosome 22 is common in patients with absent pulmonary valve syndrome | Q72340463 | ||
| P433 | issue | 4 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 1067-1071 | |
| P577 | publication date | 1997-10-01 | |
| P1433 | published in | Journal of the American College of Cardiology | Q2984355 |
| P1476 | title | Truncus arteriosus communis associated with chromosome 22q11 deletion | |
| P478 | volume | 30 |
| Q37104145 | A case report of truncus arteriosus communis and genetic counseling |
| Q49829251 | An unusual and rare form of truncus arteriosus in an asymptomatic woman |
| Q73840767 | Anatomic patterns of conotruncal defects associated with deletion 22q11 |
| Q74070188 | Association of chromosome 22q11 deletion with isolated anomalies of aortic arch laterality and branching |
| Q37219665 | Cardiac defects and results of cardiac surgery in 22q11.2 deletion syndrome |
| Q33797160 | Chromosomal abnormalities among children born with conotruncal cardiac defects |
| Q73882302 | Chromosome 22q11 deletion in patients with truncus arteriosus |
| Q51926421 | Chromosome 22q11 deletions in patients with conotruncal heart defects. |
| Q58141926 | Chromosome 22q11.2 microdeletion in children with conotruncal heart defects: frequency, associated cardiovascular anomalies, and outcome following cardiac surgery |
| Q39654228 | Clinical manifestations of Deletion 22q11.2 syndrome (DiGeorge/Velo-Cardio-Facial syndrome) |
| Q34123316 | Congenital heart disease and genetic syndromes: specific correlation between cardiac phenotype and genotype. |
| Q52319310 | Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiers. |
| Q74195745 | Deficiency of the infundibular septum in patients with interrupted aortic arch and del 22q11 |
| Q52173575 | Developmental anomalies of the outflow tracts and aortic arch: towards an understanding of the role of deletions within the 22nd chromosome. |
| Q24322838 | GATA6 mutations cause human cardiac outflow tract defects by disrupting semaphorin-plexin signaling |
| Q73118269 | Interruption of the aortic arch associated with deletion of chromosome 22q11 is associated with a subarterial and doubly committed ventricular septal defect in Japanese patients |
| Q77738871 | Isolation of the subclavian artery associated with chromosome 22q11 deletion |
| Q80428079 | Laterality of the aortic arch and anomalies of the subclavian artery-reliable indicators for 22q11.2 deletion syndromes? |
| Q64096984 | Left pulmonary artery in 22q11.2 deletion syndrome. Echocardiographic evaluation in patients without cardiac defects and role of Tbx1 in mice |
| Q30524838 | Prenatal diagnosis of truncus arteriosus using multiplanar display in 4D ultrasonography |
| Q77220992 | Right aortic arch with coarctation proximal to the right subclavian artery and Kommerell's diverticulum |
| Q46846667 | The role of modern imaging techniques in the diagnosis of malposition of the branch pulmonary arteries and possible association with microdeletion 22q11.2. |
| Q80852749 | Truncus arteriosus communis in a midtrimester fetus: comparison of prenatal ultrasound and MRI with postmortem MRI and autopsy |
| Q35597644 | Ventricular septal defects: morphology of the doubly committed juxtaarterial and muscular variants. |
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