1. A disease, probably hereditary, characterised by severe mental deficiency and a constant gross abnormality of aminoacid metabolism;Allan, J.D.; Cusworth, D.C.; Dent, C.E.; Wilson, V.K.;Lancet,1958
2. A case of congenital cirrhosis of the liver with renal tubular defects akin to those in the Fanconi syndrome;Baber, M.D.;Arch. Dis. Childh,1956
3. Hereditary pellagra-like skin rash with temporary cerebellar ataxia, constant renal amino-aciduria, and other bizarre biochemical features;Baron, D.N.; Dent, C.E.; Harris, H.; Hart, E.W.; Jepson, J.B.;Lancet,1956
4. Indicanuria in phenylketonuria;Bessman, S.P.; Tada, K.;Metabolism,1960
5. Cystine storage disease with aminoaciduria and dwarfism (Lignac-Fanconi disease);Bickel, H.; Smallwood, W.C.; Smellie, J.M.; Hickmans, E.M.;Acta paediat,1952