A PvuII polymorphism detected by pEW404 (D17S64) on chromosome 17

Por Lucas, A.M., Vance, J.M., Stajich, J.M., Roses, A.D.
Publicado em 1991

Haplotype analysis in Icelandic families defines a minimal interval for the macular corneal dystrophy type I gene.

Por Liu, N P, Baldwin, J, Jonasson, F, Dew-Knight, S, Stajich, J M, Lennon, F, Pericak-Vance, M A, Klintworth, G K, Vance, J M
Publicado em 1998

Misclassification and linkage of hereditary sensory and autonomic neuropathy type 1 as Charcot-Marie-Tooth disease, type 2B.

Por Vance, J. M., Speer, M. C., Stajich, J. M., West, S., Wolpert, C., Gaskell, P., Lennon, F., Tim, R. M., Rozear, M., Othmane, K. B.
Publicado em 1996

Evidence for anticipation in autosomal dominant limb-girdle muscular dystrophy.

Por Speer, M C, Gilchrist, J M, Stajich, J M, Gaskell, P C, Westbrook, C A, Horrigan, S K, Bartoloni, L, Yamaoka, L H, Scott, W K, Pericak-Vance, M A
Publicado em 1998

Genetic mapping of dinucleotide repeat polymorphisms and von Hippel-Lindau disease on chromosome 3p25-26.

Por Pericak-Vance, M A, Nunes, K J, Whisenant, E, Loeb, D B, Small, K W, Stajich, J M, Rimmler, J B, Yamaoka, L H, Smith, D I, Drabkin, H A
Publicado em 1993

Linkage studies in facioscapulohumeral muscular dystrophy (FSHD)

Por Gilbert, J. R., Stajich, J. M., Speer, M. C., Vance, J. M., Stewart, C. S., Yamaoka, L. H., Samson, F., Fardeau, M., Potter, T. G., Roses, A. D., Pericak-Vance, M. A.
Publicado em 1992

Identification of a new autosomal dominant limb-girdle muscular dystrophy locus on chromosome 7.

Por Speer, M C, Vance, J M, Grubber, J M, Lennon Graham, F, Stajich, J M, Viles, K D, Rogala, A, McMichael, R, Chutkow, J, Goldsmith, C, Tim, R W, Pericak-Vance, M A
Publicado em 1999

Evidence for heterogeneity in facioscapulohumeral muscular dystrophy (FSHD)

Por Gilbert, J. R., Stajich, J. M., Wall, S., Carter, S. C., Qiu, H., Vance, J. M., Stewart, C. S., Speer, M. C., Pufky, J., Yamaoka, L. H., Rozear, M., Samson, F., Fardeau, M., Roses, A. D., Pericak-Vance, M. A.
Publicado em 1993