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Publication

Clinical experience with shallow whole genome sequencing as a detection method for Copy Number Variations

Book Contribution - Book Abstract Conference Contribution

Book: EUROPEAN JOURNAL OF HUMAN GENETICS

Volume: 27

Pages: 846 - 847

WoS Id: 000489313106189
Handle: http://hdl.handle.net/1854/LU-8666015
ArticleNumber: Abstract: C19.1