Pages that link to "Q72064736"

The following pages link to Tetralogy of Fallot associated with chromosome 22q11 deletion (Q72064736):

Displaying 36 items.

• Canadian Cardiovascular Society 2009 Consensus Conference on the management of adults with congenital heart disease: outflow tract obstruction, coarctation of the aorta, tetralogy of Fallot, Ebstein anomaly and Marfan's syndrome (Q33776426) (← links)
• Congenital heart disease and genetic syndromes: specific correlation between cardiac phenotype and genotype. (Q34123316) (← links)
• The epidemiology and genetics of congenital heart disease (Q34193720) (← links)
• Extracardiac features predicting 22q11.2 deletion syndrome in adult congenital heart disease (Q35115372) (← links)
• Monosomy 22q11 in patients with pulmonary atresia, ventricular septal defect, and major aortopulmonary collateral arteries (Q35366780) (← links)
• Ductal stent implantation in tetralogy of fallot with aortic arch abnormality (Q35758831) (← links)
• Cardiac defects and results of cardiac surgery in 22q11.2 deletion syndrome (Q37219665) (← links)
• Clinical manifestations of Deletion 22q11.2 syndrome (DiGeorge/Velo-Cardio-Facial syndrome) (Q39654228) (← links)
• Congenital isolation of the subclavian artery in adults (Q40488489) (← links)
• Associated cardiac anomalies in isolated and syndromic patients with tetralogy of Fallot. (Q40986085) (← links)
• Relation of genotype 22q11 deletion to phenotype of pulmonary vessels in tetralogy of Fallot and pulmonary atresia-ventricular septal defect. (Q41912446) (← links)
• Microarray analysis reveals key genes and pathways in Tetralogy of Fallot (Q42546611) (← links)
• 22q11.2 deletion syndrome as a risk factor for aortic root dilation in tetralogy of Fallot (Q43408597) (← links)
• The incidence of a deletion in chromosome 22Q11 in sporadic and familial conotruncal heart disease (Q43821719) (← links)
• Atsuyoshi Takao (Q48547720) (← links)
• Developmental anomalies of the outflow tracts and aortic arch: towards an understanding of the role of deletions within the 22nd chromosome. (Q52173575) (← links)
• Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiers. (Q52319310) (← links)
• Surgical correction of isolated unilateral absence of right pulmonary artery (Q53280932) (← links)
• Chromosome 22q11.2 microdeletion in children with conotruncal heart defects: frequency, associated cardiovascular anomalies, and outcome following cardiac surgery (Q58141926) (← links)
• DiGeorge subtypes of nonsyndromic conotruncal defects: evidence against a major role of TBX1 Gene (Q58193810) (← links)
• Left pulmonary artery in 22q11.2 deletion syndrome. Echocardiographic evaluation in patients without cardiac defects and role of Tbx1 in mice (Q64096984) (← links)
• Cardiac anomalies associated with a chromosome 22q11 deletion in patients with conotruncal anomaly face syndrome (Q71529851) (← links)
• 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 (Q73118269) (← links)
• Truncus Arteriosus Communis Associated With Chromosome 22q11 Deletion (Q73746117) (← links)
• Anatomic patterns of conotruncal defects associated with deletion 22q11 (Q73840767) (← links)
• Tetralogy of Fallot associated with chromosome 22q11.2 deletion in adolescents and young adults (Q73840774) (← links)
• 22q11.2 microdeletions in adults with familial tetralogy of Fallot (Q73840779) (← links)
• Association of chromosome 22q11 deletion with isolated anomalies of aortic arch laterality and branching (Q74070188) (← links)
• Deficiency of the infundibular septum in patients with interrupted aortic arch and del 22q11 (Q74195745) (← links)
• Frequency of 22q11 deletions in patients with conotruncal defects (Q77107628) (← links)
• Right aortic arch with coarctation proximal to the right subclavian artery and Kommerell's diverticulum (Q77220992) (← links)
• Prenatal detection of a tetralogy of Fallot with origin of the left pulmonary artery from the ascending aorta in a familial 22q11 microdeletion (Q77346146) (← links)
• Cervical origin of the subclavian artery as a specific marker for monosomy 22q11 (Q77616520) (← links)
• Isolation of the subclavian artery associated with chromosome 22q11 deletion (Q77738871) (← links)
• NRP1 haploinsufficiency predisposes to the development of Tetralogy of Fallot (Q87601370) (← links)
• Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association (Q90669133) (← links)