RASSF1A Mutation in Myelodysplastic Syndromes by Monteiro, F.D.S, de Freitas, P. Curi, Carvalho-Salles, A.B, Ricci Junior, O, Fett-Conte, A.C

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Single nucleotide polymorphisms in the CNTNAP2 gene in Brazilian patients with autistic spectrum disorder by Nascimento, P P, Bossolani-Martins, A L, Rosan, D B A, Mattos, L C, Brandão-Mattos, C, Fett-Conte, A C

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271 - RASSF1A Mutation in Myelodysplastic Syndromes by Monteiro, F.D.S., de Freitas, P. Curi, Carvalho-Salles, A.B., Ricci Junior, O., Fett-Conte, A.C.

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MOMO syndrome associated with autism: a case report by Giunco, C T, Moretti-Ferreira, D, Silva, A E, Rocha, S S, Fett-Conte, A C

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Global gene expression profile in myelodysplastic syndromes using SAGE by Mendiburu, C F, Silva, Jr, W A, Ricci, Jr, O, Bonini-Domingos, C R, Fett-Conte, A C

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Subtelomeric region of chromosome 2 in patients with autism spectrum disorders by Barbosa-Gonçalves, A, Vendrame-Goloni, C B, Martins, A L B, Fett-Conte, A C

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Clinical outcome in chronic myeloid leukemia after allogeneic hematopoietic stem cell transplantation: the experience of the Bone Marrow Transplantation Unit of FUNFARME/BRAZIL usi... by Vendrame-Goloni, C B, Carvalho-Salles, A B, Ruiz, M A, Ricci Júnior, O, Varella-Garcia, M, Fett-Conte, A C

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Genetic study by Multiplex Ligation-dependent Probe Amplification (MLPA) in synaptic genes in autism spectrum disorders by Bossolani-Martins, A.L., Pereira-Nascimento, P., Moreira, D.P., Giunco, C.T., Passos-Bueno, M.R., Fett-Conte, A.C.

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Case Report Clonal monosomy of chromosome 21 in a case of myelodysplastic syndrome by Freitas, P.C., Carvalho-Salles, A.B., Mendiburu, C.F., Ricci Jr, O., Fett-Conte, A.C.

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Mucopolysaccharidosis type II: Identification of 30 novel mutations among Latin American patients by Brusius-Facchin, A.C., Schwartz, I.V.D., Zimmer, C., Ribeiro, M.G., Acosta, A.X., Horovitz, D., Monlleó, I.L., Fontes, M.I.B., Fett-Conte, A., Sobrinho, R.P. Oliveira, Duarte, A.R., Boy, R., Mabe, P., Ascurra, M., de Michelena, M., Tylee, K.L., Besley, G.T.N., Garreton, M.C.V., Giugliani, R., Leistner-Segal, S.

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