Multilocus Family-Based Association Analysis of Seven Candidate Polymorphisms with Essential Hypertension in an African-Derived Semi-Isolated Brazilian Population
Kimura, L., Angeli, C. B., Auricchio, M. T. B. M., Fernandes, G. R., Pereira, A. C., Vicente, J. P., Pereira, T. V., Mingroni-Netto, R. C.
Published in International Journal of Hypertension (01.01.2012)
Published in International Journal of Hypertension (01.01.2012)
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Genomic copy number alterations in non-syndromic hearing loss
Rosenberg, C., Freitas, É. L., Uehara, D. T., Auricchio, M. T. B. M., Costa, S. S., Oiticica, J., Silva, A. G., Krepischi, A. C., Mingroni-Netto, R. C.
Published in Clinical genetics (01.04.2016)
Published in Clinical genetics (01.04.2016)
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Aberrant transcript produced by a splice donor site deletion in the TECTA gene is associated with autosomal dominant deafness in a Brazilian family
Lezirovitz, Karina, Batissoco, Ana C., Lima, Fernanda T., Auricchio, Maria T.B.M., Nonose, Renata W., dos Santos, Simone R., Guilherme, Luiza, Oiticica, Jeanne, Mingroni-Netto, Regina C.
Published in Gene (15.12.2012)
Published in Gene (15.12.2012)
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A novel autosomal dominant deafness locus (DFNA58) maps to 2p12-p21
Lezirovitz, K, Braga, MCC, Thiele-Aguiar, RS, Auricchio, MTBM, Pearson, PL, Otto, PA, Mingroni-Netto, RC
Published in Clinical genetics (01.05.2009)
Published in Clinical genetics (01.05.2009)
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A novel missense mutation p.L76P in the GJB2 gene causing nonsyndromic recessive deafness in a Brazilian family
Batissoco, A C, Auricchio, M T B M, Kimura, L, Tabith-Junior, A, Mingroni-Netto, R C
Published in Brazilian journal of medical and biological research (01.02.2009)
Published in Brazilian journal of medical and biological research (01.02.2009)
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Chromosome imbalances in syndromic hearing loss
Catelani, ALPM, Krepischi, ACV, Kim, CA, Kok, F, Otto, PA, Auricchio, MTBM, Mazzeu, JF, Uehara, DT, Costa, SS, Knijnenburg, J, Tabith Jr, A, Vianna-Morgante, AM, Mingroni-Netto, RC, Rosenberg, C
Published in Clinical genetics (01.11.2009)
Published in Clinical genetics (01.11.2009)
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Correspondence regarding Ballana et al., “Mitochondrial 12S rRNA gene mutations affect RNA secondary structure and lead to variable penetrance in hearing impairment”
Abreu-Silva, R.S., Batissoco, A.C., Lezirovitz, K., Romanos, J., Rincon, D., Auricchio, M.T.B.M., Otto, P.A., Mingroni-Netto, R.C.
Published in Biochemical and biophysical research communications (12.05.2006)
Published in Biochemical and biophysical research communications (12.05.2006)
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