Probable identity by descent and discovery of familial relationships by means of a rare β-thalassemia haplotype
- 1 January 1997
- journal article
- case report
- Published by Hindawi Limited in Human Mutation
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- Genetic analysis of type 1 diabetes using whole genome approaches.Proceedings of the National Academy of Sciences, 1995
- Genetic Dissection of Complex TraitsScience, 1994
- Sporadic alleles, including a novel mutation, characterize β-thalassemia in ashkenazi jewsHuman Mutation, 1993
- Improved detection of ?-thalassaemia carriers by a two-test methodHuman Genetics, 1977