1. Lesch-Nyhan syndrome: preventive control by prenatal diagnosis;Boyle, J.A.; Raivio, K.O.; Astrin, K.H.; Schulman, J.D.; Graf, M.L.; Seegmiller, J.E.; Jacobsen, C.B.;Science,1970
2. Biochemical diagnosis of an Xlinked disease in utero;Fujimoto, W.Y.; Seegmiller, J.E.; Uhlendorf, B.W.; Jacobson, C.B.;Lancet,1968
3. Transport and storage of amniotic fluid samples for prenatal diagnosis of metabolic diseases;Niermeijer, M.F.; Halley, D.; Sachs, E.S.; TichelaarKlepper, C.; L, Garver K.;Humangenetik,1973
4. Rapid tissue culture and microbiochemical methods for analyzing colonially grown fibroblasts from normal, Lesch-Nyhan and TaySachs patients and amniotic fluid cells;Richardson, B.I.; Cox, D.M.;Clinical Genetics,1973
5. Preventive control of the LeschNyhan syndrome;van Heeswijk, P.J.; Blank, C.H.; Seegmiller, J.E.; Jacobsen, C.B.;Obstetrics and Gynecology,1972