| Hannes FD, Sharp AJ, Mefford HC, de Ravel T, Ruivenkamp CA, Breuning MH, Fryns JP, Devriendt K, Van Buggenhout G, Vogels A, Stewart H, Hennekam RC, Cooper GM, Regan R, Knight SJ, Eichler EE, Vermeesch JR, Recurrent reciprocal deletions and duplications of 16p1311: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant Journal of medical genetics46:223-32 2008 |