A novel missense mutation p.L76P in the GJB2 gene causing nonsyndromic recessive deafness in a Brazilian family

by A.C. Batissoco, M.T.B.M. Auricchio, L. Kimura, A. Tabith-Junior, R.C. Mingroni-Netto
Published 2009-02-01

<a name="home"></a>Prevalence of the A1555G (12S rRNA) and tRNA Ser(UCN) mitochondrial mutations in hearing-impaired Brazilian patients

by R.S. Abreu-Silva, K. Lezirovitz, M.C.C. Braga, M. Spinelli, S. Pirana, V.A. Della-Rosa, P.A. Otto, R.C. Mingroni-Netto
Published 2006-02-01

Multilocus Family-Based Association Analysis of Seven Candidate Polymorphisms with Essential Hypertension in an African-Derived Semi-Isolated Brazilian Population

by L. Kimura, C. B. Angeli, M. T. B. M. Auricchio, G. R. Fernandes, A. C. Pereira, J. P. Vicente, T. V. Pereira, R. C. Mingroni-Netto
Published 2012-01-01

Transplantation and survival of mouse inner ear progenitor/stem cells in the organ of Corti after cochleostomy of hearing-impaired guinea pigs: preliminary results

by L.C.M. Barboza Jr., K. Lezirovitz, D.B. Zanatta, B.E. Strauss, R.C. Mingroni-Netto, J. Oiticica, L.A. Haddad, R.F. Bento
Published 2016-01-01

Association of polymorphisms at the ADIPOR1 regulatory region with type 2 diabetes and body mass index in a Brazilian population with European or African ancestry

by E. Yeh, L. Kimura, F.I.V. Errera, C.B. Angeli, R.C. Mingroni-Netto, M.E.R. Silva, L.H.S. Canani, M.R. Passos-Bueno
Published 2008-06-01