Results of next-generation sequencing gene panel diagnostics including copy-number variation analysis in 810 patients suspected of heritable thoracic aortic disorders

Author(s):
Overwater, E.; Marsili, L.; Baars, M.J.H.; Baas, A.F.; Beek, I. van de; Dulfer, E.; Hagen, J.M. van; Hilhorst-Hofstee, Y.; Kempers, M.; Krapels, I.P.; Menke, L.A.; Verhagen, J.M.A.; Yeung, K.K.; Zwijnenburg, P.J.G.; Groenink, M.; Rijn, P. van; Weiss, M.M.; Voorhoeve, E.; Tintelen, J.P. van; Houweling, A.C.; Maugeri, A.
Published
2018
Publication type
Article / Letter to editor
copy-number variationseXome hidden Markov modelgeneticsthoracic aortic aneurysmthoracic aortic dissection
Date issued
2018-09-30
Language
English
Is part of
Human Mutation (2018), Vol. 39, no. 9, p. 1173-1192
hdl
1887/86500
doi
10.1002/humu.23565
URL
https://onlinelibrary.wiley.com/doi/epdf/10.1002/humu.23565