Congenital Heart Disease : Molecular Diagnostics /
| Autor Corporativo: | |
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| Otros Autores: | |
| Formato: | eBook |
| Lenguaje: | English |
| Publicado: |
Totowa, NJ :
Humana Press : Imprint: Humana,
2006.
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| Edición: | 1st ed. 2006. |
| Colección: | Methods in Molecular Medicine,
126 |
| Materias: |
Tabla de Contenidos:
- Genetics of Cardiac Septation Defects and Their Pre-Implantation Diagnosis
- Molecular and Genetic Aspects of DiGeorge/Velocardiofacial Syndrome
- Mutation Screening for the Genes Causing Cardiac Arrhythmias
- Mutation Analysis of the FBN1 Gene in Patients With Marfan Syndrome
- Mutation Analysis of PTPN11 in Noonan Syndrome by WAVE
- Williams-Beuren Syndrome Diagnosis Using Fluorescence In Situ Hybridization
- Congenital Heart Disease
- “Chip”ping Away at Heart Failure
- Molecular Diagnostics of Catecholaminergic Polymorphic Ventricular Tachycardia Using Denaturing High-Performance Liquid Chromatography and Sequencing
- Mutation Detection in Tumor Suppressor Genes Using Archival Tissue Specimens
- Friedreich Ataxia
- The Cardiovascular Manifestations of Alagille Syndrome and JAG1 Mutations
- Array Analysis Applied to Malformed Hearts
- DNA Mutation Analysis in Heterotaxy
- Use of Denaturing High-Performance Liquid Chromatography to Detect Mutations in Pediatric Cardiomyopathies.