Adults with Congenital Heart Disease

[1]  R. Hinton,et al.  The family history: reemergence of an established tool. , 2008, Critical care nursing clinics of North America.

[2]  A. Cook,et al.  Structural heart defects associated with an increased nuchal translucency: 9 years experience in a referral centre , 2008, Prenatal diagnosis.

[3]  A. Tsalenko,et al.  The fine-scale and complex architecture of human copy-number variation. , 2008, American journal of human genetics.

[4]  A. De Paepe,et al.  Ehlers-Danlos syndromes and Marfan syndrome. , 2008, Best practice & research. Clinical rheumatology.

[5]  Michael J Ackerman,et al.  Inherited Arrhythmias: A National Heart, Lung, and Blood Institute and Office of Rare Diseases Workshop Consensus Report About the Diagnosis, Phenotyping, Molecular Mechanisms, and Therapeutic Approaches for Primary Cardiomyopathies of Gene Mutations Affecting Ion Channel Function , 2007, Circulation.

[6]  T. de Ravel,et al.  Submicroscopic chromosomal imbalances detected by array-CGH are a frequent cause of congenital heart defects in selected patients. , 2007, European heart journal.

[7]  D. Srivastava,et al.  Genetic basis for congenital heart defects: current knowledge: a scientific statement from the American Heart Association Congenital Cardiac Defects Committee, Council on Cardiovascular Disease in the Young: endorsed by the American Academy of Pediatrics. , 2007, Circulation.

[8]  K. Sermon,et al.  Preimplantation genetic diagnosis for cancer predisposition syndromes , 2007, Prenatal diagnosis.

[9]  M. Digilio,et al.  Familial recurrence of congenital heart disease: an overview and review of the literature , 2006, European Journal of Pediatrics.

[10]  R. Hinton,et al.  Congenital heart disease: Genetic causes and developmental insights , 2005 .

[11]  W. McKenna,et al.  New insights into the pathology of inherited cardiomyopathy , 2005, Heart.

[12]  L. Feuk,et al.  Detection of large-scale variation in the human genome , 2004, Nature Genetics.

[13]  C. Basson,et al.  Preimplantation genetic diagnosis of human congenital heart malformation and Holt–Oram syndrome , 2004, American journal of medical genetics. Part A.

[14]  E. Blennow,et al.  Subtelomeric rearrangements detected in patients with idiopathic mental retardation. , 2002, American journal of medical genetics.

[15]  R. Nussbaum,et al.  Genetic Counseling and Risk Assessment , 2007 .

[16]  C. Basson,et al.  Genetics of cardiac septation defects and their pre-implantation diagnosis. , 2006, Methods in molecular medicine.