Estudo genético-clínico e molecular da síndrome de Waardenburg (SW) (1999)
- Authors:
- USP affiliated authors: BUENO, MARIA RITA DOS SANTOS E PASSOS - IB ; OTTO, PAULO ALBERTO - IB
- Unidade: IB
- Assunto: GENÉTICA MÉDICA
- Language: Português
- Imprenta:
- Publisher: Sociedade Brasileira de Genética
- Publisher place: Ribeirão Preto
- Date published: 1999
- Source:
- Título do periódico: Genetics and Molecular Biology
- Volume/Número/Paginação/Ano: v. 22, n. 3, suppl., p. 239-240, oct. 1999
- Conference titles: Congresso Nacional de Genética
-
ABNT
PARDONO, Eliete et al. Estudo genético-clínico e molecular da síndrome de Waardenburg (SW). Genetics and Molecular Biology. Ribeirão Preto: Sociedade Brasileira de Genética. . Acesso em: 19 abr. 2024. , 1999 -
APA
Pardono, E., Iughetti, P., Passos-Bueno, M. R., & Otto, P. A. (1999). Estudo genético-clínico e molecular da síndrome de Waardenburg (SW). Genetics and Molecular Biology. Ribeirão Preto: Sociedade Brasileira de Genética. -
NLM
Pardono E, Iughetti P, Passos-Bueno MR, Otto PA. Estudo genético-clínico e molecular da síndrome de Waardenburg (SW). Genetics and Molecular Biology. 1999 ; 22( 3): 239-240.[citado 2024 abr. 19 ] -
Vancouver
Pardono E, Iughetti P, Passos-Bueno MR, Otto PA. Estudo genético-clínico e molecular da síndrome de Waardenburg (SW). Genetics and Molecular Biology. 1999 ; 22( 3): 239-240.[citado 2024 abr. 19 ] - Screening of c934g and c937g mutations among patients with craniosynostosis reveals two apert patients not caused by any of these mutations
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