You are seeing this message because your Web browser does not support basic Web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.


Advertisement

ABOUT ARCHIVES
Advanced Search

Welcome   | My Account | E-mail Alerts | Access Rights | Sign In


Congenital Heart Defects

1 Citation displayed.

Most recent content (12 Nov 2001):

Original Investigations
Genotype and Phenotype Analysis of 171 Patients Referred for Molecular Study of the Fibrillin-1 Gene FBN1 Because of Suspected Marfan Syndrome
Bart Loeys; Lieve Nuytinck; Isabelle Delvaux; Sylvia De Bie; Anne De Paepe
Arch Intern Med 2001; 161: 2447-2454. [Abstract] [Full text] [PDF]  

 Collections
 •Sign up for Topic Collection Alerts
 •Topic Collections Home
 • Show Congenital Heart Defects
 collections from JAMA & Archives Journals.
 •Related collections:
  •Cardiovascular System
  •Arrhythmias
  •Cardiovascular Disease/ Myocardial Infarction
  •Congenital Heart Defects
  •Congestive Heart Failure/ Cardiomyopathy
  •Cardiac Diagnostic Tests
  •Cardiovascular Interventions
  •Venous Thromboembolism
  •Cardiovascular System, Other
Advertisement





HOME | CURRENT ISSUE | PAST ISSUES | TOPIC COLLECTIONS | CME | SUBMIT | SUBSCRIBE | HELP
CONDITIONS OF USE | PRIVACY POLICY | CONTACT US | SITE MAP
 
© 2009 American Medical Association. All Rights Reserved.