Characterization of a recurrent 15q24 microdeletion syndrome.
Sharp AJ; Selzer RR; Veltman JA; Gimelli S; Gimelli G; Striano P; Coppola A; Regan R; Price SM; Knoers NV; Eis PS; Brunner HG; Hennekam RC; Knight SJ; de Vries BB; Zuffardi O; Eichler EE; Human Molecular Genetics, 2007, vol. 16, issue 5, p 567, ISSN 09646906. ISBN 09646906.

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