Bibliotecas PUC-SP - Busca Integrada

Hereditary motor and sensory neuropathies.

von Vance, J M
Veröffentlicht 1991

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

von Lucas, A.M., Vance, J.M., Stajich, J.M., Roses, A.D.
Veröffentlicht 1991

Partitioned pulsed-field gel electrophoresis-PCR (PPF-PCR): a new method for pulsed-field mapping for STS and microsatellites.

von Denton, P H, Cullen, J B, Loeb, D, Lucas, A, Nunes, K, Hulett, C, Vance, J M
Veröffentlicht 1994

Linkage of a gene for macular corneal dystrophy to chromosome 16.

von Vance, J. M., Jonasson, F., Lennon, F., Sarrica, J., Damji, K. F., Stauffer, J., Pericak-Vance, M. A., Klintworth, G. K.
Veröffentlicht 1996

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

von 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.
Veröffentlicht 1996

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

von 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
Veröffentlicht 1998

Linkage studies in peripheral neurofibromatosis.

von Pericak-Vance, M A, Yamaoka, L H, Vance, J M, Aylsworth, A S, Rossenwasser, G O, Gaskell, P C, Alberts, M J, Hung, W Y, Haynes, C, Roses, A D
Veröffentlicht 1987

Linkage studies in facioscapulohumeral muscular dystrophy (FSHD)

von 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.
Veröffentlicht 1992

Mild and severe muscular dystrophy caused by a single gamma-sarcoglycan mutation.

von McNally, E. M., Passos-Bueno, M. R., Bönnemann, C. G., Vainzof, M., de Sá Moreira, E., Lidov, H. G., Othmane, K. B., Denton, P. H., Vance, J. M., Zatz, M., Kunkel, L. M.
Veröffentlicht 1996

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

von 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
Veröffentlicht 1999

LONGITUDINAL FOLLOW-UP OF LATE-ONSET ALZHEIMER DISEASE FAMILIES

von Carney, R.M., Slifer, M.A., Lin, P.I., Gaskell, P. C., Scott, W. K., Potocky, C.F., Hulette, C. M., Welsh-Bohmer, K. A., Schmechel, D. E., Vance, J.M., Pericak-Vance, M. A.
Veröffentlicht 2008

Evidence for heterogeneity in facioscapulohumeral muscular dystrophy (FSHD)

von 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.
Veröffentlicht 1993

Polymorphisms of the Tumor Suppressor Gene LSAMP are Associated with Left Main Coronary Artery Disease

von Wang, L., Hauser, E. R., Shah, S. H., Seo, D., Sivashanmugam, P., Exum, S. T., Gregory, S. G., Granger, C. B., Haines, J. L., Jones, C. J. H., Crossman, D., Haynes, C., Kraus, W. E., Freedman, N. J., Pericak-Vance, M. A., Goldschmidt-Clermont, P. J., Vance, J. M.
Veröffentlicht 2008

Heteroduplex molecules formed between allelic sequences cause nonparental RAPD bands.

von Ayliffe, M A, Lawrence, G J, Ellis, J G, Pryor, A J, Fujita, N, Mori, H, Yura, T, Ishihama, A, Lefrère, V, Duncan, R F, Beyert, N, Reichenberger, S, Peters, M, Hartung, M, Göttlich, B, Goedecke, W, Vielmetter, W, Pfeiffer, P, Wada, M, Abe, K, Okumura, K, Taguchi, H, Kohno, K, Imamoto, F, Schlessinger, D, Kuwano, M, Zwilling, S, Annweiler, A, Wirth, T, Ghosh, A, Ghosh, T, Ghosh, S, Das, S, Adhya, S, Klungland, A, Bjørås, M, Hoff, E, Seeberg, E, Kuiken, G A, Bertens, P J, Peterson-Maduro, J, Veenstra, G J, Koster, J G, Destrée, O H, Marguet, E, Forterre, P, Wu, H, Jiang, L, Zimmermann, R A, Shu, H H, Stuart, K, Wehnert, M S, Matson, R S, Rampal, J B, Coassin, P J, Caskey, C T, Berkhout, B, van Hemert, F J, Manna, F, Massardo, D R, Wolf, K, Luccarini, G, Carlomagno, M S, Rivellini, F, Alifano, P, Del Giudice, L, Sedensky, M M, Hudson, S J, Everson, B, Morgan, P G, Hu, J, Xu, Y, Schappert, K, Harrington, T, Wang, A, Braga, R, Mogridge, J, Friesen, J D, Han, J, Hsu, C, Zhu, Z, Longshore, J W, Finley, W H, Robertson, R W, Zhang, L, Pasco, D S, Fagan, J B, Zhang, M Q, Marr, T G, Birch-Hirschfeld, E, Földes-Papp, Z, Gührs, K H, Seliger, H, Granato, M, Schnabel, H, Schnabel, R, Li, F, Barnathan, E S, Karikó, K, Byth, B C, Thomas, G R, Hofland, N, Cox, D W, Sassano, M, Repetto, M, Cassani, G, Corti, A, McClelland, M, Arensdorf, H, Cheng, R, Welsh, J, Guidet, F, Wang, L, Hirayasu, K, Ishizawa, M, Kobayashi, Y, Denton, P H, Cullen, J B, Loeb, D, Lucas, A, Nunes, K, Hulett, C, Vance, J M, Bendixen, C, Gangloff, S, Rothstein, R, Penner, G A, Bezte, L J, Ramsden, D A, Baetz, K, Wu, G E, Eldrup, A B, Bjergårde, K, Felding, J, Kehler, J, Dahl, O, Sadofsky, M J, Hesse, J E, Gellert, M, Cuomo, C A, Oettinger, M A, Chiba, H, Muramatsu, M, Nomoto, A, Kato, H, Arvidson, D N, Arvidson, C G, Lawson, C L, Miner, J, Adams, C, Youderian, P, Heard, E, Avner, P, Rothstein, R, Toutant, M, Gauthier-Rouviere, C, Fiszman, M Y, Lemonnier, M, Chow, C W, Clark, M, Rinaldo, J, Chalkley, R, Rojo, F, Alonso, J C, Enríquez, J A, Ramos, J, Pérez-Martos, A, López-Pérez, M J, Montoya, J, Winters, T A, Henner, W D, Russell, P S, McCullough, A, Jorgensen, T J, Hadjiagapiou, C, Giannoni, F, Funahashi, T, Skarosi, S F, Davidson, N O, Jäschke, A, Fürste, J P, Erdmann, V A, Cech, D, Goller, M, Funke, B, Gehe-Becker, C, Kröger, B, Lottspeich, F, Horak, I, Wong, J M, Bateman, E, Takeshita, M, Eisenberg, W, Merino, E, Balbás, P, Puente, J L, Bolívar, F, Mayfield, C, Miller, D
Veröffentlicht 1994