Homogeneous Multiplex Genotyping of Hemochromatosis Mutations with Fluorescent Hybridization Probes
- 1 October 1998
- journal article
- research article
- Published by Elsevier in The American Journal of Pathology
- Vol. 153 (4), 1055-1061
- https://doi.org/10.1016/s0002-9440(10)65650-7
Abstract
No abstract availableKeywords
This publication has 40 references indexed in Scilit:
- Haplotype Analysis of Hemochromatosis: Evaluation of Different Linkage-Disequilibrium Approaches and Evolution of Disease ChromosomesAmerican Journal of Human Genetics, 1997
- Enhanced discrimination of single nucleotide polymorphisms by artificial mismatch hybridizationNature Biotechnology, 1997
- An evaluation of selected DNA extraction strategies for short tandem repeat typingElectrophoresis, 1997
- A novel MHC class I–like gene is mutated in patients with hereditary haemochromatosisNature Genetics, 1996
- Database of mutations in the p53 and APC tumor suppressor genes designed to facilitate molecular epidemiological analysesHuman Mutation, 1996
- A Comprehensive Human Linkage Map with Centimorgan DensityScience, 1994
- DNA Probes: Applications of the Principles of Nucleic Acid HybridizationCritical Reviews in Biochemistry and Molecular Biology, 1991
- Prevalence of Hemochromatosis among 11,065 Presumably Healthy Blood DonorsNew England Journal of Medicine, 1988
- Idiopathic HemochromatosisNew England Journal of Medicine, 1977
- Association of HLA-A3 and HLA-B14 antigens with idiopathic haemochromatosis.Gut, 1976