Use of PCR in the Diagnosis of Monogenic Disease
- 1 January 1989
- book chapter
- Published by Springer Nature
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- Diagnosis of Sickle Cell Anemia and β-Thalassemia with Enzymatically Amplified DNA and Nonradioactive Allele-Specific Oligonucleotide ProbesNew England Journal of Medicine, 1988
- Further studies of gene deletions that cause Duchenne and Becker muscular dystrophiesGenomics, 1988
- Direct detection of more than 50% of the Duchenne muscular dystrophy mutations by field inversion gelsNature, 1987
- Detection and sequence of mutations in the factor VIII gene of haemophiliacsNature, 1985
- Prenatal Diagnosis of β-ThalassemiaNew England Journal of Medicine, 1983
- Improved Detection of the Sickle Mutation by DNA AnalysisNew England Journal of Medicine, 1982
- A Sensitive New Prenatal Test for Sickle-Cell AnemiaNew England Journal of Medicine, 1982
- Use of restriction endonucleases for mapping the allele for beta s-globin.Proceedings of the National Academy of Sciences, 1982
- Organization of the alpha-globin genes in the Chinese alpha-thalassemia syndromes.Journal of Clinical Investigation, 1979
- Polymorphism of DNA sequence adjacent to human beta-globin structural gene: relationship to sickle mutation.Proceedings of the National Academy of Sciences, 1978