Novel mutations of PAX3, MITF and SOX10 genes found in Waardenburg syndrome types 1 and 2 in Brazilian patients (2013)
- Authors:
- USP affiliated authors: NETTO, REGINA CELIA MINGRONI - IB ; OTTO, PAULO ALBERTO - IB
- Unidade: IB
- Subjects: PIGMENTOS (ANORMALIDADES); PELE (ANORMALIDADES); PERDA AUDITIVA; ÍRIS (ANORMALIDADES); MUTAÇÃO GENÉTICA
- Language: Inglês
- Imprenta:
- Publisher: Sociedade Brasileira de Genática - SBG
- Publisher place: Ribeirão Preto
- Date published: 2013
- ISBN: 978-85-89109-06-2
- Source:
- Título do periódico: Resumos
- Conference titles: Congresso Brasileiro de Genética
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ABNT
PRETTEL BOCANGEL, M. A e MINGRONI NETTO, Regina Celia e OTTO, Paulo A. Novel mutations of PAX3, MITF and SOX10 genes found in Waardenburg syndrome types 1 and 2 in Brazilian patients. 2013, Anais.. Ribeirão Preto: Sociedade Brasileira de Genática - SBG, 2013. Disponível em: http://web2.sbg.org.br/congress/sbg2008/pdfs2013/GH.pdf. Acesso em: 23 abr. 2024. -
APA
Prettel Bocangel, M. A., Mingroni Netto, R. C., & Otto, P. A. (2013). Novel mutations of PAX3, MITF and SOX10 genes found in Waardenburg syndrome types 1 and 2 in Brazilian patients. In Resumos. Ribeirão Preto: Sociedade Brasileira de Genática - SBG. Recuperado de http://web2.sbg.org.br/congress/sbg2008/pdfs2013/GH.pdf -
NLM
Prettel Bocangel MA, Mingroni Netto RC, Otto PA. Novel mutations of PAX3, MITF and SOX10 genes found in Waardenburg syndrome types 1 and 2 in Brazilian patients [Internet]. Resumos. 2013 ;[citado 2024 abr. 23 ] Available from: http://web2.sbg.org.br/congress/sbg2008/pdfs2013/GH.pdf -
Vancouver
Prettel Bocangel MA, Mingroni Netto RC, Otto PA. Novel mutations of PAX3, MITF and SOX10 genes found in Waardenburg syndrome types 1 and 2 in Brazilian patients [Internet]. Resumos. 2013 ;[citado 2024 abr. 23 ] Available from: http://web2.sbg.org.br/congress/sbg2008/pdfs2013/GH.pdf - A previously undescribed syndrome combining fibular agenesis/hypoplasia, oligodactylous clubfeet, anonychia/ungual hypoplasia, and other defects
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