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

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

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190

Citations

43

References

2018

Year

Alba Sanchis‐Juan, Jonathan Stephens, Courtney E. French, Nicholas Gleadall, Karyn Mégy, Christopher J. Penkett, Olga Shamardina, Kathleen Stirrups, Isabelle Delon, Eleanor Dewhurst,

Genome Medicine

References

	Year	Citations

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