PGD for translocations – increased risk for multiple chromosomal abnormalities von Okada, L, Sanseverino, M.T, Azambuja, R, Tagliani-Ribeiro, A, Badalotti, M, Petracco, A

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P-52 PGD for translocations – increased risk for multiple chromosomal abnormalities von Sanseverino, M.T, Okada, L, Ribeiro, A, Azambuja, R, Reig, V, Kvitko, D, Michelon, J, Petracco, R, Badalotti, F, Petacco, A, Badalotti, M

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P034 Prevalence of cystic fibrosis paediatric patients with p.Arg1162X mutation in southern Brazil: a migration flow outcome von Sanseverino, P.B., Farias, M., Michels, M., Sanseverino, M.T., Marostica, P.J.

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P199 Cystic fibrosis plus systemic lupus: a relation of inflammatory diseases von Sanseverino, P., Farias, M., Michels, M., Sanseverino, M.T., Marostica, P.J.

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Supplementary Material for: New SHH and Known SIX3 Variants in a Series of Latin American Patients with Holoprosencephaly von V.F., deCastro, D., Mattos, F.M., deCarvalho, D.P., Cavalcanti, M.M., Duenas-Roque, J., LlerenaJr, V.R., Cosentino, R.S., Honjo, J.C.L., Leite, M.T., Sanseverino, M.P.A., deSouza, P., Bernardi, A.M., Bolognese, L.C., SantanadaSilva, P., Barbero, P.S., Correia, L.S.M., Bueno, C.P., Savastano, I.M., Orioli

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