Clinical and Molecular Characterization of an Infant with a Tandem Duplication and Deletion of 19p13

Tan, R.N.G.B.; Witlox, R.S.G.M.; Hilhorst-Hofstee, Y.; Peeters-Scholte, C.M.P.C.D.; Hollander, N.S. den; Ruivenkamp, C.A.L.; ... ; Santen, G.W.E. (2015)

Article / Letter to editor

• chromosome 19 duplication and deletion
• mate-pair sequencing
• congenital heart disease
• refractory edema

• All authors: Tan, R.N.G.B.; Witlox, R.S.G.M.; Hilhorst-Hofstee, Y.; Peeters-Scholte, C.M.P.C.D.; Hollander, N.S. den; Ruivenkamp, C.A.L.; Hoffer, M.J.V.; Hansson, K.B.; Roosmalen, M.J. van; Kloosterman, W.P.; Santen, G.W.E.
• Date: 2015-08-31
• Journal: American Journal of Medical Genetics Part A
• Volume: 167
• Issue: 8
• Pages: 1884 - 1889
• DOI: doi:10.1002/ajmg.a.37076