Interstitial deletion del(3)(p12p21) in a malformed child subsequent to paternal paracentric insertion (or intraarm shift) 46,XY, ins(3)(p24.1p12.1p21.31) - Pfeiffer, R A; Rauch, A; Ulmer, R; Beinder, E; Trautmann, U (Ann Genet, 1998)