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Genomic copy number alterations in non-syndromic hearing loss.
Published in:
Clinical Genetics, 2016, v. 89, n. 4, p. 473, doi. 10.1111/cge.12683
By:
- 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.
Publication type:
Article
Chromosome imbalances in syndromic hearing loss.
Published in:
Clinical Genetics, 2009, v. 76, n. 5, p. 458, doi. 10.1111/j.1399-0004.2009.01276.x
By:
- Catelani, A. L. P. M.;
- Krepischi, A. C. V.;
- Kim, C. A.;
- Kok, F.;
- Otto, P. A.;
- Auricchio, M. T. B. M.;
- Mazzeu, J. F.;
- Uehara, D. T.;
- Costa, S. S.;
- Knijnenburg, J.;
- Tabith Jr., A.;
- Vianna-Morgante, A. M.;
- Mingroni-Netto, R. C.;
- Rosenberg, C.
Publication type:
Article
Transplantation and survival of mouse inner ear progenitor/stem cells in the organ of Corti after cochleostomy of hearing-impaired guinea pigs: preliminary results.
Published in:
Brazilian Journal of Medical & Biological Research, 2016, v. 49, n. 4, p. 1, doi. 10.1590/1414-431X20155064
By:
- Barboza Jr., L. C. M.;
- Lezirovitz, K.;
- Zanatta, D. B.;
- Strauss, B. E.;
- Mingroni-Netto, R. C.;
- Oiticica, J.;
- Haddad, L. A.;
- Bento, R. F.
Publication type:
Article
Cochlea cell-specific marker expression upon in vitro Hes1 knockdown.
Published in:
Brazilian Journal of Medical & Biological Research, 2021, v. 54, n. 7, p. 1, doi. 10.1590/1414-431X2020e10579
By:
- Batissoco, A. C.;
- Lezirovitz, K.;
- Zanatta, D. B.;
- Hemza, C. R. M. L.;
- Vasques, L. R.;
- Strauss, B. E.;
- Mingroni-Netto, R. C.;
- Haddad, L. A.;
- Bento, R. F.;
- Oiticica, J.
Publication type:
Article
Corrigendum to: NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss.
Published in:
Human Molecular Genetics, 2022, v. 31, n. 1, p. 156, doi. 10.1093/hmg/ddab325
By:
- Salazar-Silva, R;
- Dantas, Vitor Lima Goes;
- Alves, Leandro Ucela;
- Batissoco, Ana Carla;
- Oiticica, Jeanne;
- Lawrence, Elizabeth A;
- Kawafi, Abdelwahab;
- Yang, Yushi;
- Nicastro, Fernanda Stávale;
- Novaes, Beatriz Caiuby;
- Hammond, Chrissy;
- Kague, Erika;
- Mingroni-Netto, R C
Publication type:
Article
Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterations.
Published in:
Cytogenetic & Genome Research, 2006, v. 115, n. 3/4, p. 254, doi. 10.1159/000095922
By:
- Krepischi-Santos, A. C. V.;
- Vianna-Morgante, A. M.;
- Jehee, F. S.;
- Passos-Bueno, M. R.;
- Knijnenburg, J.;
- Szuhai, K.;
- Sloos, W.;
- Mazzeu, J. F.;
- Kok, F.;
- Cheroki, C.;
- Otto, P. A.;
- Mingroni-Netto, R. C.;
- Varela, M.;
- Koiffmann, C.;
- Kim, C. A.;
- Bertola, D. R.;
- Pearson, P. L.;
- Rosenberg, C.
Publication type:
Article
Multilocus Family-Based Association Analysis of Seven Candidate Polymorphisms with Essential Hypertension in an African-Derived Semi-Isolated Brazilian Population.
Published in:
2012
By:
- 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.
Publication type:
Journal Article
Multilocus Family-Based Association Analysis of Seven Candidate Polymorphisms with Essential Hypertension in an African-Derived Semi-Isolated Brazilian Population.
Published in:
International Journal of Hypertension, 2012, p. 1, doi. 10.1155/2012/859219
By:
- 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.
Publication type:
Article

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