1. 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.;Med Genet,1985
2. Partial monosomy for chromosome 22 in a patient with del( 22)(pter-+ql3.1:: ql 3.33-eqter);Romain, D.R.; Goldsmith, J.; Cairney, H.; Columbano-Green, L.M.; Smythe, R.H.; Parfitt, R.G.;Med Genet,1990
3. Multiple congenital anomaly/mental retardation (MCA/MR) syndrome with Goldenhar complex due to a terminal del(22q). AmJMed Genet;Herman, G.E.; Greenberg, F.; Ledbetter, D.H.,1988
4. Two patients with 22qI3.3 deletions have similar facies and developmental patterns;Zwaigenbaum, L.; Siegel-Bartelt, J.; Teshima, I.; Ho, C.;Am Hum Genet,1990
5. Terminal 22q deletion associated with a partial deficiency of arylsulphatase A;Narahara, K.; Takahashi, Y.; Murakami, M.;Y Med Genet,1992