SNP discovery in associating genetic variation with human disease phenotypes
Author:
Publisher
Elsevier BV
Subject
Health, Toxicology and Mutagenesis,Genetics,Molecular Biology
Reference81 articles.
1. International Human Genome Sequencing Consortium. Finishing the euchromatic sequence of the human genome, Nature 431 (2004) 931–945.
2. Mapping complex disease loci in whole-genome association studies;Carlson;Nature,2004
3. Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA;Riordan;Science,1989
4. Identification of the cystic fibrosis gene: chromosome walking and jumping;Rommens;Science,1989
5. Identification of the cystic fibrosis gene: genetic analysis;Kerem;Science,1989
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