1. Partial monosomy 18 and anomaly of thyroxine synthesis;Buhler, E.M.; Buhler, U.K.; Stalder, G.R.;Lancet,1964
2. Deletion of the long arm of chromosome 16 and an unexpected Duffy blood group phenotype reveal a possible autosomal linkage;Crawford, M.N.; Punnett, H.H.; Carpenter, G.G.;Nature (Lond.),1967
3. La deletion partielle du bras long du chromosome 18 (syndrome 18q-);Destine, M.L.; Punnett, H.H.; Thovichet, S.; DiGeorge, A.M.; Weiss, L.;Ann. Genet,1967
4. A ring D chromosome and anomalous inheritance of haptoglobulin type;Gerald, P.S.; Warner, S.; Singer, J.D.; Corcoran, P.A.; Umansky, I.;J. Pediat,1967
5. ABO frequencies in mongolism;Goodman, H.O.; Thomas, J.J.;Ann. hum. Genet,1966