Applying and testing the conveniently optimized enzyme mismatch cleavage method to clinical DNA diagnosis. [electronic resource]
Producer: 20130327Description: 580-5 p. digitalISSN:- 1096-7206
- Arthritis -- diagnosis
- Base Sequence
- Biological Assay
- Child, Preschool
- Coffin-Lowry Syndrome -- diagnosis
- Collagen Type II -- genetics
- Connective Tissue Diseases -- diagnosis
- DNA Restriction Enzymes -- metabolism
- Electrophoresis, Polyacrylamide Gel
- Exodeoxyribonucleases -- genetics
- Exons
- Hearing Loss, Sensorineural -- diagnosis
- Humans
- Infant
- Male
- Middle Aged
- Molecular Sequence Data
- Mutation
- Nucleic Acid Heteroduplexes -- analysis
- RecQ Helicases -- genetics
- Reproducibility of Results
- Retinal Detachment -- diagnosis
- Ribosomal Protein S6 Kinases, 90-kDa -- genetics
- Sensitivity and Specificity
- Silver Staining
- Werner Syndrome -- diagnosis
- Werner Syndrome Helicase
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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