Pages that link to "Q30502924"
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The following pages link to Echocardiographic evaluation of asymptomatic parental and sibling cardiovascular anomalies associated with congenital left ventricular outflow tract lesions (Q30502924):
Displaying 32 items.
- Bicuspid Aortic Valve: a Review with Recommendations for Genetic Counseling (Q28080091) (← links)
- Variants of folate metabolism genes and risk of left-sided cardiac defects (Q33814980) (← 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)
- 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) (← links)
- Is a shorter atrioventricular septal length an intermediate phenotype in the spectrum of nonsyndromic atrioventricular septal defects? (Q36059054) (← links)
- New Genetic Insights into Congenital Heart Disease (Q36106143) (← links)
- Genome-Wide Association Study of Down Syndrome-Associated Atrioventricular Septal Defects. (Q36119845) (← links)
- The Role of the Geneticist and Genetic Counselor in an ACHD Clinic (Q36292010) (← links)
- Aortic stenosis at young adult age. (Q36314868) (← 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)
- Notch signaling in cardiac development and disease. (Q37785202) (← links)
- Family-based studies to identify genetic variants that cause congenital heart defects (Q38120090) (← links)
- Impact of MYH6 variants in hypoplastic left heart syndrome. (Q38803277) (← links)
- Genetic Bases of Bicuspid Aortic Valve: The Contribution of Traditional and High-Throughput Sequencing Approaches on Research and Diagnosis (Q41537361) (← links)
- Cardiac, mandibular and thymic phenotypical association indicates that cranial neural crest underlies bicuspid aortic valve formation in hamsters (Q41980468) (← links)
- Heart malformation: what are the chances it could happen again? (Q42874167) (← links)
- Variants in the NOTCH1 gene in patients with aortic coarctation. (Q46812710) (← links)
- Whole exome sequencing in 342 congenital cardiac left sided lesion cases reveals extensive genetic heterogeneity and complex inheritance patterns (Q47128713) (← links)
- Familial Screening for Left-Sided Congenital Heart Disease: What Is the Evidence? What Is the Cost? (Q47171029) (← links)
- Familial co-occurrence of congenital heart defects follows distinct patterns (Q47437992) (← links)
- Relationship of Echocardiographic Z Scores Adjusted for Body Surface Area to Age, Sex, Race, and Ethnicity: The Pediatric Heart Network Normal Echocardiogram Database (Q47595778) (← links)
- EDUCATIONAL SERIES IN CONGENITAL HEART DISEASE: Congenital left-sided heart obstruction. (Q52313260) (← links)
- The Genetic Landscape of Hypoplastic Left Heart Syndrome. (Q52430968) (← links)
- Analysis of chromosomal structural variation in patients with congenital left-sided cardiac lesions. (Q52652397) (← links)
- Autosomal and X chromosome structural variants are associated with congenital heart defects in Turner syndrome: The NHLBI GenTAC registry. (Q52850139) (← links)
- Assessment of large copy number variants in patients with apparently isolated congenital left-sided cardiac lesions reveals clinically relevant genomic events. (Q54787395) (← links)
- Inheritance analysis of congenital left ventricular outflow tract obstruction malformations: Segregation, multiplex relative risk, and heritability. (Q55221257) (← links)
- Identification of clinically actionable variants from genome sequencing of families with congenital heart disease (Q57180807) (← links)
- Submicroscopic Chromosomal Copy Number Variations Identified in Children With Hypoplastic Left Heart Syndrome (Q57828161) (← links)