Correlation Between Genotype and Phenotype in Hereditary Hemochromatosis: Analysis of 61 Cases
- 31 August 1997
- journal article
- Published by Elsevier in Blood Cells, Molecules, and Diseases
- Vol. 23 (2) , 314-320
- https://doi.org/10.1006/bcmd.1997.0148
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Mutation Analysis in Hereditary HemochromatosisBlood Cells, Molecules, and Diseases, 1996
- A novel MHC class I–like gene is mutated in patients with hereditary haemochromatosisNature Genetics, 1996
- Hereditary hemochromatosisClinica Chimica Acta; International Journal of Clinical Chemistry, 1996
- Screening blood donors for hereditary hemochromatosis: Decision analysis model based on a 30-year databaseGastroenterology, 1995
- Screening for HemochromatosisNew England Journal of Medicine, 1993
- Identification of Homozygous Hemochromatosis Subjects by Measurement of Hepatic Iron IndexHepatology, 1990
- Screening for HemochromatosisaAnnals of the New York Academy of Sciences, 1988
- Prevalence of Hemochromatosis among 11,065 Presumably Healthy Blood DonorsNew England Journal of Medicine, 1988
- Hemochromatosis: Current Concepts and ManagementHospital Practice, 1987
- Value of Hepatic Iron Measurements in Early Hemochromatosis and Determination of the Critical Iron Level Associated With FibrosisHepatology, 1986