Deafness recurrence Risks in families excluded for connexin mutations (2010)
- Authors:
- USP affiliated authors: NETTO, REGINA CELIA MINGRONI - IB ; OTTO, PAULO ALBERTO - IB
- Unidade: IB
- Subjects: SURDEZ; DOENÇAS HEREDITÁRIAS
- Language: Inglês
- Imprenta:
- Publisher: Sociedade Brasileira de Genética (SBG)
- Publisher place: Ribeirao Preto
- Date published: 2010
- Source:
- Título: Resumos
- Conference titles: Congresso Brasileiro de Genética
-
ABNT
MINGRONI NETTO, Regina Celia et al. Deafness recurrence Risks in families excluded for connexin mutations. 2010, Anais.. Ribeirao Preto: Sociedade Brasileira de Genética (SBG), 2010. . Acesso em: 21 fev. 2026. -
APA
Mingroni Netto, R. C., Batissoco, A. C., Auricchio, M. T. B. de M., & Otto, P. A. (2010). Deafness recurrence Risks in families excluded for connexin mutations. In Resumos. Ribeirao Preto: Sociedade Brasileira de Genética (SBG). -
NLM
Mingroni Netto RC, Batissoco AC, Auricchio MTB de M, Otto PA. Deafness recurrence Risks in families excluded for connexin mutations. Resumos. 2010 ;[citado 2026 fev. 21 ] -
Vancouver
Mingroni Netto RC, Batissoco AC, Auricchio MTB de M, Otto PA. Deafness recurrence Risks in families excluded for connexin mutations. Resumos. 2010 ;[citado 2026 fev. 21 ] - Waardenburg Syndrome: description of two novel mutations in the PAX3 gene, one of which incompletely penetrant
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