Sort   by:  
 Page size 
UnknownVariants of folate metabolism genes and the risk of conotruncal cardiac defects.
Not available
S-EPMC3035562 | biostudies-literature
UnknownStaged Versus Complete Repair in the Symptomatic Neonate With Tetralogy of Fallot.
Not available
S-EPMC7054157 | biostudies-literature
UnknownImproved Outcomes in Patients with 22q11.2 Deletion Syndrome and Diagnosis of Interrupted Aortic Arch Prior to Birth Hospital Discharge, a Retrospective Study.
Not available
S-EPMC9859187 | biostudies-literature
UnknownGenetic variants of HIF1α are associated with right ventricular fibrotic load in repaired tetralogy of Fallot patients: a cardiovascular magnetic resonance study.
Not available
S-EPMC6699069 | biostudies-literature
UnknownMutations in NTRK3 suggest a novel signaling pathway in human congenital heart disease.
Not available
S-EPMC4247247 | biostudies-literature
UnknownNAT1, NOS3, and TYMS genotypes and the risk of conotruncal cardiac defects.
Not available
S-EPMC4404296 | biostudies-literature
UnknownGene-gene interactions in the folate metabolic pathway and the risk of conotruncal heart defects.
Not available
S-EPMC2810479 | biostudies-literature
UnknownAssociation of Habitual Activity and Body Mass Index in Survivors of Congenital Heart Surgery: A Study of Children and Adolescents With Tetralogy of Fallot, Transposition of the Great Arteries, and Fontan Palliation.
Not available
S-EPMC6154798 | biostudies-literature
UnknownEvaluation of heterogeneity in the association between congenital heart defects and variants of folate metabolism genes: conotruncal and left-sided cardiac defects.
Not available
S-EPMC3257803 | biostudies-literature
UnknownMESP1 Mutations in Patients with Congenital Heart Defects.
Not available
S-EPMC4762608 | biostudies-literature
Sort   by:  
 Page size