Duplication of EYA1 causes Branchiootic Syndrome in a Brazilian family (2014)
- Authors:
- USP affiliated authors: NETTO, REGINA CELIA MINGRONI - IB ; ROSENBERG, CARLA - IB
- Unidade: IB
- Subjects: PERDA AUDITIVA; MAPEAMENTO GENÉTICO; MUTAÇÃO GENÉTICA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Abstracts
- Conference titles: Annual Meeting of the American Society of Human Genetics
-
ABNT
MINGRONI NETTO, Regina Celia et al. Duplication of EYA1 causes Branchiootic Syndrome in a Brazilian family. 2014, Anais.. Boston: Instituto de Biociências, Universidade de São Paulo, 2014. Disponível em: http://www.ashg.org/2013meeting/abstracts/fulltext/f130123586.htm. Acesso em: 21 maio 2024. -
APA
Mingroni Netto, R. C., Dantas, V. G. L., Freitas, E. L., Moraes, A. M. S. M., Braga, M. C. C., Ramos, S. B., et al. (2014). Duplication of EYA1 causes Branchiootic Syndrome in a Brazilian family. In Abstracts. Boston: Instituto de Biociências, Universidade de São Paulo. Recuperado de http://www.ashg.org/2013meeting/abstracts/fulltext/f130123586.htm -
NLM
Mingroni Netto RC, Dantas VGL, Freitas EL, Moraes AMSM, Braga MCC, Ramos SB, Rosenberg C, Della-Rosa VA. Duplication of EYA1 causes Branchiootic Syndrome in a Brazilian family [Internet]. Abstracts. 2014 ;[citado 2024 maio 21 ] Available from: http://www.ashg.org/2013meeting/abstracts/fulltext/f130123586.htm -
Vancouver
Mingroni Netto RC, Dantas VGL, Freitas EL, Moraes AMSM, Braga MCC, Ramos SB, Rosenberg C, Della-Rosa VA. Duplication of EYA1 causes Branchiootic Syndrome in a Brazilian family [Internet]. Abstracts. 2014 ;[citado 2024 maio 21 ] Available from: http://www.ashg.org/2013meeting/abstracts/fulltext/f130123586.htm - Deletion of the entire POU4F3 gene in a familial case of autosomal dominant non-syndromic hearing loss
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