Bibliotecas PUC-SP - Busca Integrada

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

af Lucas, A.M., Vance, J.M., Stajich, J.M., Roses, A.D.
Udgivet 1991

Coexistence of macular corneal dystrophy types I and II in a single sibship

af Liu, N., Baldwin, J., Lennon, F., Stajich, J., Thonar, E., Pericak-Vance, M., Klintworth, G., Vance, J.
Udgivet 1998

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

af 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.
Udgivet 1996

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

af 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
Udgivet 1998

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

af 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
Udgivet 1998

Linkage studies in facioscapulohumeral muscular dystrophy (FSHD)

af 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.
Udgivet 1992

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

af 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
Udgivet 1993

Exclusion mapping of chromosomal regions which cross hybridise to FSHD1A associated markers in FSHD1B

af Gilbert, J R, Speer, M C, Stajich, J, Clancy, R, Lewis, K, Qiu, H, Yamaoka, L, Kumar, A, Vance, J, Stewart, C, Rozear, M, Roses, A D, Pericak-Vance, M A
Udgivet 1995

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

af 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
Udgivet 1999

Evidence for heterogeneity in facioscapulohumeral muscular dystrophy (FSHD)

af 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.
Udgivet 1993