Cargando…
Genome-Wide Profiling of Structural Genomic Variations in Korean HapMap Individuals
BACKGROUND: Structural genomic variation study, along with microarray technology development has provided many genomic resources related with architecture of human genome, and led to the fact that human genome structure is a lot more complicated than previously thought. METHODOLOGY/PRINCIPAL FINDING...
Autores principales: | Bae, Joon Seol, Cheong, Hyun Sub, Park, Byung Lae, Kim, Lyoung Hyo, Han, Chang Soo, Park, Tae Joon, Kim, Jason Yongha, Pasaje, Charisse Flerida A., Lee, Jin Sol, Shin, Hyoung Doo |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2896390/ https://www.ncbi.nlm.nih.gov/pubmed/20625389 http://dx.doi.org/10.1371/journal.pone.0011417 |
Ejemplares similares
-
Identification of copy number variations and common deletion polymorphisms in cattle
por: Bae, Joon Seol, et al.
Publicado: (2010) -
WDR46 is a Genetic Risk Factor for Aspirin-Exacerbated Respiratory Disease in a Korean Population
por: Pasaje, Charisse Flerida A., et al.
Publicado: (2012) -
Association of CACNG6 polymorphisms with aspirin-intolerance asthmatics in a Korean population
por: Lee, Jin Sol, et al.
Publicado: (2010) -
Possible role of EMID2 on nasal polyps pathogenesis in Korean asthma patients
por: Pasaje, Charisse Flerida Arnejo, et al.
Publicado: (2012) -
The Genetic Effect of Copy Number Variations on the Risk of Type 2 Diabetes in a Korean Population
por: Bae, Joon Seol, et al.
Publicado: (2011)