Pages that link to "Q58193949"

The following pages link to Deletion 22q11 in patients with interrupted aortic arch (Q58193949):

Displaying 20 items.

• Isolated interrupted aortic arch: unexpected diagnosis in a 63-year-old male (Q33566031) (← links)
• 22q11.2 Deletion syndrome is associated with increased perioperative events and more complicated postoperative course in infants undergoing infant operative correction of truncus arteriosus communis or interrupted aortic arch (Q34022848) (← links)
• Congenital heart disease and genetic syndromes: specific correlation between cardiac phenotype and genotype. (Q34123316) (← links)
• Microdeletion and microduplication analysis of chinese conotruncal defects patients with targeted array comparative genomic hybridization (Q35009370) (← links)
• Cardiac defects and results of cardiac surgery in 22q11.2 deletion syndrome (Q37219665) (← links)
• Interrupted aortic arch with isolated persistent left superior vena cava in patient with Turners syndrome (Q37319796) (← links)
• The three-vessel view in the fetal mediastinum in the diagnosis of interrupted aortic arch (Q37917238) (← links)
• Congenital Thoracic Vascular Anomalies: Evaluation with State-of-the-Art MR Imaging and MDCT (Q37925924) (← links)
• Fetal and neonatal diagnosis of interrupted aortic arch: associations and outcomes (Q37957660) (← links)
• Clinical manifestations of Deletion 22q11.2 syndrome (DiGeorge/Velo-Cardio-Facial syndrome) (Q39654228) (← links)
• Dutch patients with glycogen storage disease type II show common ancestry for the 525delT and del exon 18 mutations (Q43075180) (← links)
• Congenital heart disease and genetic syndromes: new insights into molecular mechanisms. (Q51835990) (← links)
• Chromosome 22q11 deletions in patients with conotruncal heart defects (Q51926421) (← links)
• Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiers. (Q52319310) (← links)
• Left pulmonary artery in 22q11.2 deletion syndrome. Echocardiographic evaluation in patients without cardiac defects and role of Tbx1 in mice (Q64096984) (← links)
• Anatomic patterns of conotruncal defects associated with deletion 22q11 (Q73840767) (← links)
• Deficiency of the infundibular septum in patients with interrupted aortic arch and del 22q11 (Q74195745) (← links)
• Genetic predisposition to ventricular septal defect in Down syndrome (Q77150382) (← links)
• A rare association of interrupted aortic arch type C and microdeletion 22q11.2. (Q80056588) (← links)
• Complete aortic arch obstruction: interruption or aortic coarctation? (Q81518711) (← links)