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Elsevier, Genetics in Medicine, 5(21), p. 1121-1130, 2019

DOI: 10.1038/s41436-018-0295-y

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Copy-number variants in clinical genome sequencing: deployment and interpretation for rare and undiagnosed disease

This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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