1. Estimates of the frequency of chromosome abnormalities detectable in unselected newborns using moderate levels of banding;Jacobs, P.A.; Browne, C.; Gregson, N.; Joyce, C.; White, H.;J Med Genet,1992
2. High resolution R-and G-banding on the same preparation;Dutrillaux, B.; Viegas-Pequignot, E.;Hum Genet,1981
3. Chromosomal localization of human ornithine aminotransferase gene sequences to 10q26 and Xpll.2;Barrett, D.J.; Bateman, B.; Sparkes, R.S.; Mohandas, T.; Klisak, I.; Inana, G.;Invest Ophthalmol Vis Sci,1987
4. Ornithine aminotransferase-related sequences map to two nonadjacent intervals on the human X chromosome short arm;Lafreniere, R.G.; Geraghty, M.T.; Valle, D.; Shows, T.B.; Willard, H.F.;Genomics,1991
5. Human ornithineb-aminotransferase. cDNA cloning and analysis of the structural gene;Mitchell, G.A.; Looney, J.E.; Brody, L.C.;Jf Biol Chem,1988