1. Adrenoleukodystrophy: evidence for X linkage, inactivation, and selection favouring the mutant alleles;Migeon, B.R.; Moser, H.W.; Moser, A.B.; Axelman, J.; Sillence, D.; Norum, R.A.,1981
2. Adrenoleukodystrophy: phenotypic variability and implications for therapy;Moser, H.W.; Moser, A.B.; Smith, K.D.;Metab Dis,1992
3. Isolation and characterisation of a human variable copy number tandem repeat at Xcenp11.22;Fraser, N.J.; Boyd, Y.; Craig, I.,1989
4. Carrier detection in X-linked agammaglobulinemia by analysis of X-chromosome inactivation;Fearon, E.R.; Winkelstein, J.A.; Civin, C.I.; Pardoll, D.M.; Vogelstein, B.;N Engl J Med,1987
5. Female haemophilia A in a family with seeming extreme bidirectional lyonization tendency: abnormal premature X-chromosome inactivation;Ingerslev, J.; Schwartz, M.; Lamm, L.U.; Kruse, T.A.; Bukh, A.; Stenbjerg, S.;Clin Genet,1989