Modifier genes in cystic fibrosis
Author:
Publisher
Wiley
Subject
Pulmonary and Respiratory Medicine,Pediatrics, Perinatology, and Child Health
Reference64 articles.
1. Single nucleotide polymorphism genotyping: biochemistry, protocol, cost and throughput
2. Apolipoprotein E Genetic Variation and Alzheimer’s Disease
3. The common PPARγ Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes
4. Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease
5. HLA-DQB1*0201
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