Karen Snow

Null alleles at the Huntington disease locus: implications for diagnostics and CAG repeat instability.

M. Hegde, R. Faull, I. Winship, 2000, Genetic testing.

Analysis of a CGG sequence at the FMR-1 locus in fragile X families and in the general population.

S. Thibodeau, S. Erster, R. Hagerman, 1993, American journal of human genetics.

Sequence analysis of the fragile X trinucleotide repeat: implications for the origin of the fragile X mutation.

D. Schaid, S. Thibodeau, D. Tester, 1994, Human molecular genetics.