A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism
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R. Pfundt | N. de Leeuw | M. Fichera | B. D. de Vries | C. Romano | R. Regan | J. Veltman | S. Knight | H. Brunner | A. V. van Kessel | R. Kooy | E. Sistermans | N. Knoers | J. Schoumans | B. Anderlid | B. Vries | A. Schinzel | D. Koolen | A. G. Kessel | N. Leeuw | A. Baumer | E. Reyniers | Lisenka E. L. M. Vissers | L. Vissers
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