Pages that link to "Q34338168"
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The following pages link to Epidemiology of noncomplex left ventricular outflow tract obstruction malformations (aortic valve stenosis, coarctation of the aorta, hypoplastic left heart syndrome) in Texas, 1999-2001 (Q34338168):
Displaying 31 items.
- A Systematic Review on the Cost-Effectiveness of Genetic and Electrocardiogram Testing for Long QT Syndrome in Infants and Young Adults (Q26795687) (← links)
- Maternal socioeconomic status and the risk of congenital heart defects in offspring: a meta-analysis of 33 studies (Q28396576) (← links)
- Getting to the heart of the matter: epidemiology of cyanotic heart defects (Q33314084) (← links)
- Linkage analysis of left ventricular outflow tract malformations (aortic valve stenosis, coarctation of the aorta, and hypoplastic left heart syndrome). (Q34047018) (← links)
- Genetic basis of congenital cardiovascular malformations (Q34125381) (← links)
- Ethnical variations in the incidence of congenital heart defects in gorgan, northern iran: a single-center study (Q34778399) (← links)
- Genome-Wide DNA Methylation Analysis and Epigenetic Variations Associated with Congenital Aortic Valve Stenosis (AVS). (Q36010819) (← links)
- The prevalence of 16p12.1 microdeletion in patients with left-sided cardiac lesions. (Q36073004) (← links)
- Bicuspid aortic valve and thoracic aortic aneurysm: three patient populations, two disease phenotypes, and one shared genotype (Q36210512) (← links)
- Cardiac teratogenicity in mouse maternal phenylketonuria: defining phenotype parameters and genetic background influences (Q36417290) (← links)
- Association of common variants in ERBB4 with congenital left ventricular outflow tract obstruction defects (Q37078059) (← links)
- NOTCH1 mutations in individuals with left ventricular outflow tract malformations reduce ligand-induced signaling (Q37294787) (← links)
- A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20. (Q37367970) (← links)
- Utilization of Whole Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart Disease. (Q38390118) (← links)
- NOTCH1 missense alleles associated with left ventricular outflow tract defects exhibit impaired receptor processing and defective EMT. (Q38570387) (← links)
- Birth outcomes of cases with left-sided obstructive defects of the heart in the function of maternal socio-demographic factors: a population-based case-control study (Q40051235) (← links)
- Folic acid fortification and the birth prevalence of congenital heart defect cases in Alberta, Canada (Q43931355) (← links)
- Is the prevalence of specific types of congenital heart defects different for non-Hispanic white, non-Hispanic black and Hispanic infants? (Q44213733) (← links)
- Risk factors in the origin of congenital left-ventricular outflow-tract obstruction defects of the heart: a population-based case-control study (Q46404500) (← links)
- Whole exome sequencing in 342 congenital cardiac left sided lesion cases reveals extensive genetic heterogeneity and complex inheritance patterns (Q47128713) (← links)
- The Genetic Landscape of Hypoplastic Left Heart Syndrome. (Q52430968) (← links)
- Quantification of congenital aortic valve stenosis in pediatric patients: comparison between cardiac magnetic resonance imaging and transthoracic echocardiography. (Q54431304) (← links)
- The association between race/ethnicity and major birth defects in the United States, 1999-2007 (Q57100551) (← links)
- Maternal age and prevalence of isolated congenital heart defects in an urban area of the United States (Q64127646) (← links)
- Changing Epidemiology of Hypoplastic Left Heart Syndrome: Results of a National Swedish Cohort Study (Q64239213) (← links)
- The severe end of the spectrum: Hypoplastic left heart in Potocki‐Lupski syndrome (Q83309410) (← links)
- De novo and recessive forms of congenital heart disease have distinct genetic and phenotypic landscapes (Q90781433) (← links)
- Transplantation-free survival after Norwood surgery for hypoplastic left heart syndrome with aortic atresia: A Swedish national cohort study (Q92532622) (← links)
- Patient-specific genomics and cross-species functional analysis implicate LRP2 in hypoplastic left heart syndrome (Q100418595) (← links)
- Social determinants of health and outcomes for children and adults with congenital heart disease: a systematic review (Q100696970) (← links)
- Maternal folic acid supplementation mediates the associations between maternal socioeconomic status and congenital heart diseases in offspring (Q101469852) (← links)