Molecular Diagnosis of Genetic Diseases

Optimizing PCR for Clinical Diagnosis.- Current and Emerging Techniques for Diagnostic Mutation Detection.- Mutation Scanning for the Clinical Laboratory.- Mutation Scanning for the Clinical Laboratory-Protein Truncation Test.- Mutation Scanning for the Clinical Laboratory.- Comparative Sequence Analysis.- Gene Dosage Analysis by Multiplex Amplifiable Probe Hybridization.- Prenatal Detection of Chromosome Aneuploidy by Quantitative Fluorescence-PCR.- Fragile X Disease.- Huntington’s Disease.- Hematological Applications.- Cystic Fibrosis.- Familial Adenomatous Polyposis.- Multiple Endocrine Neoplasia Types 1 and 2.- Neurofibromatosis Type 1.- Duchenne and Becker Muscular Dystrophy.- Spinal Muscular Atrophy.- Quality Management in Molecular Genetics.- Regulation of Genetic Testing in Clinical Practice.