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Refinado por: autor: Mingroni-Netto, R remover
Result Number Material Type Add to My Shelf Action Record Details and Options
1
c.G2114A MYH9 mutation (DFNA17) causes non-syndromic autosomal dominant hearing loss in a Brazilian family
c.G2114A MYH9 mutation (DFNA17) causes non-syndromic autosomal dominant hearing loss in a Brazilian family
Material Type:
Artigo 		Adicionar ao Meu Espaço

c.G2114A MYH9 mutation (DFNA17) causes non-syndromic autosomal dominant hearing loss in a Brazilian family

Vitor G. L. Dantas Karina Lezirovitz; Guilherme L Yamamoto; Carolina Fischinger Moura de Souza; Simone Gomes Ferreira; Regina Celia Mingroni Netto

Genetics and Molecular Biology Ribeirão Preto online, p. on-line, 2014

Ribeirão Preto 2014

Item não circula. Consulte sua biblioteca.(Acessar)

2
Mutation analysis of SLC26A4 (Pendrin) gene in a Brazilian sample of hearing- impaired subjects
Mutation analysis of SLC26A4 (Pendrin) gene in a Brazilian sample of hearing- impaired subjects
Material Type:
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Mutation analysis of SLC26A4 (Pendrin) gene in a Brazilian sample of hearing- impaired subjects

Renata Watanabe Nonose Karina Lezirovitz; Maria Teresa Balester De Mello Auricchio; Ana Carla Batissoco; Guilherme Lopes Yamamoto; Regina Celia Mingroni Netto

BMC Medical Genetics London v. 19, art. 73, p. 1-10, May 2018

London 2018

Item não circula. Consulte sua biblioteca.(Acessar)

3
Characterization of a novel MYO3A missense mutation associated with a dominant form of late onset hearing loss
Characterization of a novel MYO3A missense mutation associated with a dominant form of late onset hearing loss
Material Type:
Artigo 		Adicionar ao Meu Espaço

Characterization of a novel MYO3A missense mutation associated with a dominant form of late onset hearing loss

Vitor G. L Dantas Dantas1, Manmeet H Raval; Angela Ballesteros; Runjia Cui; Laura K Gunther; Guilherme L Yamamoto; Leandro Ucela Alves; André Silva Bueno; Karina Lezirovitz; Sulene Pirana; Beatriz C. A Mendes; Christopher M Yengo; Bechara Kachar; Regina Celia Mingroni Netto

Scientific Reports London v. 8, art. 8706, p. 1-15, June 2018

London 2018

Item não circula. Consulte sua biblioteca.(Acessar)

4
Author Correction whole-genome sequencing of 1,171 elderly admixed individuals from Brazil
Author Correction whole-genome sequencing of 1,171 elderly admixed individuals from Brazil
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Artigo 		Adicionar ao Meu Espaço

Author Correction whole-genome sequencing of 1,171 elderly admixed individuals from Brazil

Michel Naslavsky Marilia O Scliar; Guilherme L Yamamoto; Jaqueline Yu Ting Wang; Stepanka Zverinova; Tatiana Karp; Kelly Nunes; José Ricardo Magliocco Ceroni; Diego Lima de Carvalho; Carlos Eduardo da Silva Simões; Daniel Bozoklian; Ricardo Nonaka; Nayane dos Santos Brito Silva; Andreia da Silva Souza; Heloísa de Souza Andrade; Marília Rodrigues Silva Passos; Camila Ferreira Bannwart Castro; Celso T Mendes-Junior; Rafael L. V Mercuri; Thiago L. A Miller; Jose Leonel Buzzo; Fernanda O Rego; Nathalia M Araújo; Wagner C. S Magalhães; Regina Celia Mingroni Netto; Victor Borda; Heinner Guio; Carlos P Rojas; Cesar Sanchez; Omar Caceres; Michael Dean; Mauricio L Barreto; Maria Fernanda Lima-Costa; Bernardo L Horta; Eduardo Tarazona-Santos; Diogo Meyer; Pedro A. F Galante; Victor Guryev; Erick C Castelli; Yeda Aparecida de Oliveira Duarte; Maria Rita Passos-Bueno; Mayana Zatz

Nature London v. 13, n. 1831, on-line, 2022

London 2022

Item não circula. Consulte sua biblioteca.(Acessar)

5
Whole-genome sequencing of 1,171 elderly admixed individuals from Brazil
Whole-genome sequencing of 1,171 elderly admixed individuals from Brazil
Material Type:
Artigo 		Adicionar ao Meu Espaço

Whole-genome sequencing of 1,171 elderly admixed individuals from Brazil

Michel Naslavsky Marilia O Scliar; Guilherme L Yamamoto; Jaqueline Yu Ting Wang; Stepanka Zverinova; Tatiana Karp; Kelly Nunes; José Ricardo Magliocco Ceroni; Diego Lima de Carvalho; Carlos Eduardo da Silva Simões; Daniel Bozoklian; Ricardo Nonaka; Nayane dos Santos Brito Silva; Andreia da Silva Souza; Heloísa de Souza Andrade; Marília Rodrigues Silva Passos; Camila Ferreira Bannwart Castro; Celso T Mendes-Junior; Rafael L. V Mercuri; Thiago L. A Miller; Jose Leonel Buzzo; Fernanda O Rego; Nathalia M Araújo; Wagner C. S Magalhães; Regina Celia Mingroni Netto; Victor Borda; Heinner Guio; Carlos P Rojas; Cesar Sanchez; Omar Caceres; Michael Dean; Mauricio L Barreto; Maria Fernanda Lima-Costa; Bernardo L Horta; Eduardo Tarazona-Santos; Diogo Meyer; Pedro A. F Galante; Victor Guryev; Erick C Castelli; Yeda Aparecida de Oliveira Duarte; Maria Rita Passos-Bueno; Mayana Zatz

Nature London v. 13, n. 1004, on-line, 2022

London 2022

Item não circula. Consulte sua biblioteca.(Acessar)

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Deste Autor:

  1. Yamamoto, G
  2. Mingroni-Netto, R
  3. Lezirovitz, K
  4. Castro, C
  5. Rego, F

Neste Assunto:

  1. Genomas
  2. Mutação Genética
  3. Miscigenação
  4. Surdez
  5. Sequenciamento Genético

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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