1. Mendelian inheritance in man;McKusick, V.A.,1978
2. Calculation of genetic risks in Duchenne muscular dystrophy by geneticists in the United Kingdom;Bundey, S.;JMed Genet,1978
3. Carrier detection in Hunter syndrome;Archer, I.M.; Young, I.D.; Rees, D.W.; Oladimeji, A.; Wusteman, F.S.; Harper, P.S.;Am JMed Genet,1983
4. The Hunter syndrome in females: is there an autosomal recessive form of iduronate sulfatase deficiency?;Neufeld, E.F.; Liebaers, I.; Epstein, C.J.; Yatziv, S.; Milunsky, A.; Migeon, B.R.;Am J Hum Genet,1977
5. Abnormal X chromosomes in man: origin, behaviour and effects;Therman, E.; Patau, K.;Humangenetik,1974