Rapid Visualisation of Microarray Copy Number Data for the Detection of Structural Variations Linked to a Disease Phenotype
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https://figshare.com/articles/dataset/Rapid_Visualisation_of_Microarray_Copy_Number_Data_for_the_Detection_of_Structural_Variations_Linked_to_a_Disease_Phenotype/121001
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Whilst the majority of inherited diseases have been found to be caused by single base substitutions, small insertions or deletions (
创建时间：
2016-01-19
