1. DiGeorge anomaly associated with partial deletion of chromosome 22. Report of a case with X/22 translocation and review of the literature;Dallapiccola, B.; Marino, B.; Giannottia, A.; Valorani, G.;Ann Genet (Paris),1989
2. A familial pericentric inversion of chromosome 22 with a recombinant subject illustrating a 'pure' partial monosomy syndrome;Watt, J.L.; Olson, I.A.; Johnston, A.W.; Ross, H.S.; Couzin, D.A.; Stephen, G.S.;J Med Genet,1985
3. Long arm deletion of chromosome 22;Kirshenbaum, G.; Chmura, M.; Rhone, D.P.;J Med Genet,1988
4. Multiple congenital anomaly/mental retardation (MCA/MR) syndrome with Goldenhar complex due to terminal del (22q);Herman, G.E.; Greenberg, F.; Ledbetter, D.H.;Am J Med Genet,1988
5. Identification by fluorescent microscopy of the abnormal chromosomes associated with the G-deletion syndrome;Warren, R.J.; Rimoin, D.L.; Summitt, R.L.;AmJI Hum Genet,1973