1. Larger expansions of the CTG repeat in muscle compared to lymphocytes from patients with myotonic dystrophy;Anvret;Hum Mot Genet,1993
2. Autosomal dominant cerebellar ataxia with retinal degeneration (ADCA type 2) is genetically different from ADCA type I;Benomar;Ann Neural,1994
3. Androgene receptor locus on the X chromosome: regional localization to Xg11–12 and description of a DNA polymorphism;Brown;Am J Hunt Genet,1989
4. Influence of sex of the transmiting parent as well as of parental allele size on the CTG expansion in myotonic dystrophy (DM);Brunner;Am J Hum Genet,1993
5. Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy;Buxton;Nature,1992