Complex structural variants in Mendelian disorders: identification and breakpoint resolution using short- and long-read genome sequencing

Overview of attention for article published in Genome Medicine, December 2018

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Open Access UCL Research: Complex structural variants in Mendelian disorders: identification and breakpoint resolution using short- and long-read genome sequencing https://t.co/YvlWqTNT40

03 Apr 2019

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09 Feb 2019

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22 Jan 2019

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