1. Progressive muscular dystrophy. II. Biochemical identification of the carrier state in the recessive sex-linked juvenile (Duchenne) type by serum creatine-phosphokinase determinations;Aebi, U.; Richterich, R.; Colombo, J.P.; Rossi, E.;Enzym. biol. clin,1961
2. Zur Genetik der Myopathien;Becker, P.E.;Dtsch. Z. Nervenheilk,1955
3. Muscular dystrophy in childhood. The genetic aspect. A field study in the Leeds region of clinical types and their inheritance;Blyth, H.; Pugh, R.J.;Ann hum. Genet,1959
4. Serum enzymes and genetic carriers in muscular dystrophy;Chung, C.S.; Morton, N.E.; Peters, H.A.;Amer. J. hum. Genet,1960
5. Serum aldolase and the diagnosis of myopathy;Evans, J.H.; Baker, R.W.R.;Brain,1957