Negligible validation rate for public domain stop-codon SNPs
- 31 July 2003
- journal article
- letter
- Published by Hindawi Limited in Human Mutation
- Vol. 22 (3) , 252-254
- https://doi.org/10.1002/humu.10256
Abstract
Click on the article title to read more.Keywords
This publication has 12 references indexed in Scilit:
- iFRET: An Improved Fluorescence System for DNA-Melting AnalysisGenome Research, 2002
- The Structure of Haplotype Blocks in the Human GenomeScience, 2002
- HGVbase: a human sequence variation database emphasizing data quality and a broad spectrum of data sourcesNucleic Acids Research, 2002
- Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's diseaseNature, 2001
- A frameshift mutation in NOD2 associated with susceptibility to Crohn's diseaseNature, 2001
- Linkage Disequilibrium and Allele-Frequency Distributions for 114 Single-Nucleotide Polymorphisms in Five PopulationsAmerican Journal of Human Genetics, 2000
- Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasisNature Genetics, 1999
- DNA sequence diversity in a 9.7-kb region of the human lipoprotein lipase geneNature Genetics, 1998
- Novel Alleles of the Chemokine-Receptor Gene CCR5American Journal of Human Genetics, 1997
- A lipoprotein lipase mutation (Asn291Ser) is associated with reduced HDL cholesterol levels in premature atherosclerosisNature Genetics, 1995