A common missense mutation in the adhalin gene in three unrelated Brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy von Bueno, M.Rita Passos, Moreira, Eloísa S., Vainzof, Mariz, Chamberlain, Jeffrey, Marle, Suely K., Pereira, Lygia, Akiyama, Jeanne, Roberds, Steven L., Campbell, Kevin P., Zatz, Mayana

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Absence of calpain 3 in a form of limb-girdle muscular dystrophy (LGMD2A) von Spencer, Melissa J, Tidball, James G, Anderson, Louise V.B, Bushby, Kate M.D, Harris, John B, Passos-Bueno, M.Rita, Somer, Hannu, Vainzof, Mariz, Zatz, Mayana

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Confirmation of the 2p Locus for the Mild Autosomal Recessive Limb-Girdle Muscular Dystrophy Gene (LGMD2B) in Three Families Allows Refinement of the Candidate Region von Passos-Bueno, M.Rita, Bashir, Ramaisa, Moreira, Eloisa S., Vainzof, Mariz, Marie, Suely K., Vasquez, Luciana, Iughetti, Paula, Bakker, Egbert, Keers, Sharon, Stephenson, Anthea, Strachan, Tom, Mahneh, Ibrahim, Weissenbach, Jean, Bushby, Katharine, Zatz, Mayana

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No evidence of genetic heterogeneity in Brazilian facioscapulohumeral muscular dystrophy familes (FSHD) with 4q markers von Passos-Bueno, M.Rita, Wijmenga, Cisca, Takata, Reinaldo E., Marie, Sueli K.N., Vainzof, Mariz, Pavanello, Rita C., Hewitt, Jane E., Bakker, Egbert, Carvalho, Alzira, Akiyama, Jane, Frants, Rune R., Zatz, Mayana

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Genetic heterogeneity for Duchenne-like muscular dystrophy (DLMD) based on linkage and 50 DAG analysis von Passos-Bueno, M.Rita, Oilvelra, Joāo R., Bakker, Egbert, Anderson, Richard D., Marie, Sueli K., Vainzof, Mariz, Roberts, Steven, Campbell, Kevin P., Zatz, Mayana

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Exclusion of the gene responsible for facioscapulohumeral muscular dystrophy (FSH) at 6q23-q27 von Passos-Bueno, M.Rita, Byth, Barbara, Love, Donald, Terwilliger, Joseph, Ott, Jurg, Rapaport, Debora, Vainzof, Mariz, Zatz, Mayana, Davies, Kay E.

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