1. First report of mosaic trisomy 12 in a liveborn individual;Patil, SR, Bosch; EP, Hanson; J.W.;Am 7 Med Genet,1983
2. Trisomy 12 mosaicism in amniocytes and dysmorphic child despite normal chromosomes in fetal blood;H, Von Koskull; A, Ritvanen; P, Ammala; N, Gahmberg; R, Salonen,1989
3. Karyotyping urine sediment cells confirms trisomy 12 mosaicism detected at amniocentesis;Leschot, N.J.; Wilmsen-Linders, E.J.M.; Van Geijn, H.P.; Samson, J.F.; Smit, L.M.E.,1988
4. Trisomy 15 with loss of the paternal 15 as a cause of Prader-Willi syndrome due to maternal disomy;Cassidy, S.B.; Lai, L.W.; Erickson, R.P.;Am J Hum Genet,1992