Molecular Diagnosis of Genetic Diseases
| Corporate Author: | |
|---|---|
| Other Authors: | |
| Format: | eBook |
| Language: | English |
| Published: |
Totowa, NJ :
Humana Press : Imprint: Humana,
1996.
|
| Edition: | 1st ed. 1996. |
| Series: | Methods in Molecular Medicine,
5 |
| Subjects: | |
| Online Access: | https://doi.org/10.1385/0896033465 |
Table of Contents:
- An Overview of Clinical Molecular Genetics
- PCR Techniques for Deletion, Linkage, and Mutation Analysis in Duchenne/Becker Muscular Dystrophy
- Detection of Unstable Trinucleotide Repeats
- Searching for Mutations
- Methods for Screening in Cystic Fibrosis
- Characterization of Gene Rearrangements and Gene Conversion Events in the 21-Hydroxylase Gene
- Molecular Analysis of X-Chromosome Inactivation
- Risk Analysis
- Hemoglobinopathies
- Automated Genotyping in Diagnosis
- Genetic Counseling and Molecular Testing
- Molecular Approaches to the Detection of Deletions and Uniparental Disomy in Prader-Willi and Angelman Syndromes
- Noninvasive Prenatal Diagnosis Using Fetal Cells in Maternal Blood
- PCR from Single Cells for Preimplantation Diagnosis
- FISH in Preimplantation Diagnosis
- Microtiter Array Diagonal Gel Electrophoresis (MADGE) for Population Scale Genotype Analyses
- Pulsed Field Gel Electrophoresis for Detection of Gene Rearrangements in Duchenne Muscular Dystrophy
- Fluorescent Sequencing Protocols in Diagnosis
- High Throughput Modifications of Single-Strand Conformation Polymorphism Analysis
- Quality Assurance in Molecular Diagnosis.