Plagnol, V (2010) A genome-wide copy number variant association study for eight common disorders in 16,000 cases and 3,000 controls. In: (Proceedings) European Society of Human Genetics.
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| Type: | Proceedings paper |
|---|---|
| Title: | A genome-wide copy number variant association study for eight common disorders in 16,000 cases and 3,000 controls |
| Event: | European Society of Human Genetics |
| Location: | Gotenborg, Sweden |
| UCL classification: | UCL > School of Life and Medical Sciences > Faculty of Life Sciences > Biosciences (Division of) > Genetics, Evolution and Environment > UCL Genetics Institute |
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