Congenital Heart Disease

- Introduction
D. Woodrow Benson

- Genetics of Cardiac Septation Defects and Their Pre-Implantation Diagnosis
Deborah A. McDermott, Craig T. Basson, and Cathy J. Hatcher

- Molecular and Genetic Aspects of DiGeorge/Velocardiofacial Syndrome
Deborah A. Driscoll

- Mutation Screening for the Genes Causing Cardiac Arrhythmias
Jeffrey A. Towbin

- Mutation Analysis of the FBN1 Gene in Patients With Marfan Syndrome
Paul Coucke, Petra Van Acker, and Anne De Paepe

- Mutation Analysis of PTPN11 in Noonan Syndrome by WAVE
Navaratnam Elanko and Steve Jeffery

- Williams-Beuren Syndrome Diagnosis Using Fluorescence In Situ Hybridization
Lucy R. Osborne, Ann M. Joseph-George, and Stephen W. Scherer

- Congenital Heart Disease: Molecular Diagnostics of Supravalvular Aortic Stenosis
May Tassabehji and Zsolt Urban

- 'Chip'ping Away at Heart Failure
J. David Barrans and Choong-Chin Liew

- Molecular Diagnostics of Catecholaminergic Polymorphic Ventricular Tachycardia Using Denaturing High-Performance Liquid Chromatography and Sequencing
Alex V. Postma, Zahurul A. Bhuiyan, and Hennie Bikker

- Mutation Detection in Tumor Suppressor Genes Using Archival Tissue Specimens
Aristotelis Astrinidis and Elizabeth Petri Henske

- Friedreich Ataxia: Detection of GAA Repeat Expansions and Frataxin Point Mutations
Massimo Pandolfo

- The Cardiovascular Manifestations of Alagille Syndrome and JAG1 Mutations
Elizabeth Goldmuntz, Elizabeth Moore, and Nancy B. Spinner

- Array Analysis Applied to Malformed Hearts: Molecular Dissection of Tetralogy of Fallot
Silke Sperling

- DNA Mutation Analysis in Heterotaxy
Stephanie M. Ware

- Use of Denaturing High-Performance Liquid Chromatography to Detect Mutations in Pediatric Cardiomyopathies
Amy J. Sehnert

- Index