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Mariguela, T.C., Ortí, G., Avelino, G.S., Abe, K.T., Oliveira, C.
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Published in Molecular phylogenetics and evolution (01.07.2013)
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P1.21 Dystrophinopathy in girls due to X-autosome translocations
Brandao, I.C.S, Abe, K.T, Monteiro, A, Antunes, J.S, Formigli, L.M, Schneider, M, Martins, C.E.S, Carvalho, D.R, Oliveira, I.M.P, Silva, C.C, Kalil, R.K
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Published in Neuromuscular disorders : NMD (01.10.2011)
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A novel stop codon mutation in the PMP22 gene associated with a variable phenotype
Abe, K.T, Lino, A.M.M, Hirata, M.T.A, Pavanello, R.C.M, Brotto, M.W.I, Marchiori, P.E, Zatz, M
Published in Neuromuscular disorders : NMD (01.05.2004)
Published in Neuromuscular disorders : NMD (01.05.2004)
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