A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism.
Koolen DA; Vissers LE; Pfundt R; de Leeuw N; Knight SJ; Regan R; Kooy RF; Reyniers E; Romano C; Fichera M; Schinzel A; Baumer A; Anderlid BM; Schoumans J; Knoers NV; van Kessel AG; Sistermans EA; Veltman JA; Brunner HG; de Vries BB; Nature Genetics, 2006, vol. 38, issue 9, p 999, ISSN 10614036. ISBN 10614036.

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