Increased prevalence of inherited neuromuscular disorders due to endogamy in Northeast Brazil: the need of community genetics services (2014)
- Authors:
- Autor USP: KOK, FERNANDO - FM
- Unidade: FM
- DOI: 10.1007/s12687-013-0174-9
- Subjects: DOENÇAS NEUROMUSCULARES (INCIDÊNCIA;ETIOLOGIA); BRASILEIROS; SERVIÇOS DE SAÚDE COMUNITÁRIA (GENÉTICA)
- Language: Inglês
- Imprenta:
- Publisher place: Heidelberg
- Date published: 2014
- Source:
- Título: Journal of Community Genetics
- ISSN: 1868-310X
- Volume/Número/Paginação/Ano: v. 5, n. 3, p. 199-203, 2014
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
SANTOS, Silvana et al. Increased prevalence of inherited neuromuscular disorders due to endogamy in Northeast Brazil: the need of community genetics services. Journal of Community Genetics, v. 5, n. 3, p. 199-203, 2014Tradução . . Disponível em: https://doi.org/10.1007/s12687-013-0174-9. Acesso em: 04 mar. 2026. -
APA
Santos, S., Pequeno, A. A. da S., Pessoa, A., Galvão, C. R. C., Medeiros, J. L. A. de, Mathias, W., & Kok, F. (2014). Increased prevalence of inherited neuromuscular disorders due to endogamy in Northeast Brazil: the need of community genetics services. Journal of Community Genetics, 5( 3), 199-203. doi:10.1007/s12687-013-0174-9 -
NLM
Santos S, Pequeno AA da S, Pessoa A, Galvão CRC, Medeiros JLA de, Mathias W, Kok F. Increased prevalence of inherited neuromuscular disorders due to endogamy in Northeast Brazil: the need of community genetics services [Internet]. Journal of Community Genetics. 2014 ; 5( 3): 199-203.[citado 2026 mar. 04 ] Available from: https://doi.org/10.1007/s12687-013-0174-9 -
Vancouver
Santos S, Pequeno AA da S, Pessoa A, Galvão CRC, Medeiros JLA de, Mathias W, Kok F. Increased prevalence of inherited neuromuscular disorders due to endogamy in Northeast Brazil: the need of community genetics services [Internet]. Journal of Community Genetics. 2014 ; 5( 3): 199-203.[citado 2026 mar. 04 ] Available from: https://doi.org/10.1007/s12687-013-0174-9 - Clinical presentation of a complex neurodevelopmental disorder caused by mutations in ADNP
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Informações sobre o DOI: 10.1007/s12687-013-0174-9 (Fonte: oaDOI API)
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