Cargando…
Candidate Genes and Single Nucleotide Polymorphisms (SNPs) in the Study of Human Disease
The genomic revolution has generated an extraordinary resource, the catalog of variation within the human genome, for investigating biological, evolutionary and medical questions. Together with new, more efficient platforms for high-throughput genotyping, it is possible to begin to dissect genetic c...
Autor principal: | Chanock, Stephen |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
IOS Press
2001
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3850582/ https://www.ncbi.nlm.nih.gov/pubmed/11673655 http://dx.doi.org/10.1155/2001/858760 |
Ejemplares similares
-
In Silico Analysis of Single Nucleotide Polymorphism (SNPs) in Human β-Globin Gene
por: Alanazi, Mohammed, et al.
Publicado: (2011) -
In silico analysis of single nucleotide polymorphisms (SNPs) in human FOXC2 gene
por: Nimir, Mohammed, et al.
Publicado: (2017) -
Single nucleotide polymorphisms (SNPs) in coding regions of canine dopamine- and serotonin-related genes
por: Våge, Jørn, et al.
Publicado: (2008) -
Comparison of microsatellites, single-nucleotide polymorphisms (SNPs) and composite markers derived from SNPs in linkage analysis
por: Xing, Chao, et al.
Publicado: (2005) -
Impact of Single Nucleotide Polymorphisms (SNPs) on Immunosuppressive Therapy in Lung Transplantation
por: Ruiz, Jesus, et al.
Publicado: (2015)