Pages that link to "Q46812710"

The following pages link to Variants in the NOTCH1 gene in patients with aortic coarctation. (Q46812710):

Displaying 14 items.

• Bioengineering and Stem Cell Technology in the Treatment of Congenital Heart Disease (Q26799556) (← links)
• Primary-care management of patients with coarctation of the aorta (Q30238662) (← links)
• Embryonic Development of the Bicuspid Aortic Valve (Q33708015) (← links)
• NOTCH 1 Mutation in a Patient with Spontaneous and Recurrent Dissections of Extracranial Arteries. (Q33780719) (← links)
• Candidate Gene Resequencing in a Large Bicuspid Aortic Valve-Associated Thoracic Aortic Aneurysm Cohort: SMAD6 as an Important Contributor. (Q33792221) (← links)
• Familial aortic coarctation: a rare cause of refractory hypertension in the elderly: a case report (Q36153269) (← links)
• NOTCH1 Mutations in Aortic Stenosis: Association with Osteoprotegerin/RANK/RANKL. (Q37633121) (← links)
• Coronary anatomy as related to bicuspid aortic valve morphology (Q40917308) (← links)
• A rare missense mutation in MYH6 associates with non-syndromic coarctation of the aorta. (Q52625501) (← links)
• Loss of function, missense, and intronic variants in NOTCH1 confer different risks for left ventricular outflow tract obstructive heart defects in two European cohorts (Q90238024) (← links)
• A novel de novo dominant mutation of NOTCH1 gene in an Iranian family with non-syndromic congenital heart disease (Q92195486) (← links)
• Chronic inflammation: A key role in degeneration of bicuspid aortic valve (Q92457243) (← links)
• Coarctation of the aorta in twins with severe hypertension (Q92481589) (← links)
• Bicuspid Aortic Valve Alters Aortic Protein Expression Profile in Neonatal Coarctation Patients (Q93159606) (← links)