Approaches to identify genes for complex human diseases: Lessons from Mendelian disorders
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference91 articles.
1. A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Starqardt macular dystrophy
2. Further Evidence for an Association of ABCR Alleles with Age-Related Macular Degeneration
3. Simple and Complex ABCR: Genetic Predisposition to Retinal Disease
4. Genomewide Scans of Complex Human Diseases: True Linkage Is Hard to Find
5. Guilt by association
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