1. 46,XY,-9,der(9),t(3;9) (p21.33;p22.1)mat
2. 46,XY,-9,der(9),t(7;9) (q31. 1;p23)pat
3. der(9), t(4; 9) (?; p24)pat lead to the complete loss of function of the gene product is not clear. In the four reported cases involving a familial translocation, the translocation was derived from the mother in two cases23 and the father in two cases.46 This makes imprinting unlikely."9;XY, -9
4. A gene from the human sex-determining region encodes a protein with homology to a conserved DNA binding motif;Sinclair, A.H.; Berta, P.; Palmer, M.S.;Nature,1990
5. A new case of trisomy for the distal part of 13q due to maternal translocation, t(9; 1 3) (p21; q21) Hum Genet;Jotterand, M.; Juillard, E.,1976