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Filtros : "PERDA AUDITIVA" "2019" Removido: "Brasil" Limpar

Filtros

USP affiliated authors
- bento, ricardo ferreira (~1)
- dias, alex marcel moreira (~1)
- netto, regina celia mingroni (~1)
Date published
- 2019 (~2)
Subjects
- perda auditiva (2)
- aconselhamento genético (1)
- editorial (1)
- indicadores de saúde (1)
- mutação genética (1)

Artigo de periodico-carta/editorial
Hearing health [Editorial]: a major concern for the 21st century (2019)
Bento, Ricardo Ferreira ; Sousa, Natalia Candido de
Source: International archives of otorhinolaryngology. Unidade: FM
Subjects: PERDA AUDITIVA, INDICADORES DE SAÚDE, PREVALÊNCIA, EDITORIAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BENTO, Ricardo Ferreira e SOUSA, Natalia Candido de. Hearing health [Editorial]: a major concern for the 21st century. International archives of otorhinolaryngology. Stuttgart: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1055/s-0039-1692980. Acesso em: 28 set. 2024. , 2019
APA
Bento, R. F., & Sousa, N. C. de. (2019). Hearing health [Editorial]: a major concern for the 21st century. International archives of otorhinolaryngology. Stuttgart: Faculdade de Medicina, Universidade de São Paulo. doi:10.1055/s-0039-1692980
NLM
Bento RF, Sousa NC de. Hearing health [Editorial]: a major concern for the 21st century [Internet]. International archives of otorhinolaryngology. 2019 ; 23( 3): E254-E255.[citado 2024 set. 28 ] Available from: https://doi.org/10.1055/s-0039-1692980
Vancouver
Bento RF, Sousa NC de. Hearing health [Editorial]: a major concern for the 21st century [Internet]. International archives of otorhinolaryngology. 2019 ; 23( 3): E254-E255.[citado 2024 set. 28 ] Available from: https://doi.org/10.1055/s-0039-1692980
Artigo de periodico
Further evidence for loss-of-function mutations in the CEACAM16 gene causing nonsyndromic autosomal recessive hearing loss in humans (2019)
Dias, Alex Marcel Moreira; Lezirovitz, Karina ; Nicastro, Fernanda Stávale; Mendes, Beatriz C. A; Mingroni Netto, Regina Celia
Source: Journal of Human Genetics. Unidade: IB
Subjects: PERDA AUDITIVA, SURDEZ, SEQUENCIAMENTO GENÉTICO, ACONSELHAMENTO GENÉTICO, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DIAS, Alex Marcel Moreira et al. Further evidence for loss-of-function mutations in the CEACAM16 gene causing nonsyndromic autosomal recessive hearing loss in humans. Journal of Human Genetics, v. 64, p. 257–260, 2019Tradução . . Disponível em: https://doi.org/10.1038/s10038-018-0546-4. Acesso em: 28 set. 2024.
APA
Dias, A. M. M., Lezirovitz, K., Nicastro, F. S., Mendes, B. C. A., & Mingroni Netto, R. C. (2019). Further evidence for loss-of-function mutations in the CEACAM16 gene causing nonsyndromic autosomal recessive hearing loss in humans. Journal of Human Genetics, 64, 257–260. doi:10.1038/s10038-018-0546-4
NLM
Dias AMM, Lezirovitz K, Nicastro FS, Mendes BCA, Mingroni Netto RC. Further evidence for loss-of-function mutations in the CEACAM16 gene causing nonsyndromic autosomal recessive hearing loss in humans [Internet]. Journal of Human Genetics. 2019 ; 64 257–260.[citado 2024 set. 28 ] Available from: https://doi.org/10.1038/s10038-018-0546-4
Vancouver
Dias AMM, Lezirovitz K, Nicastro FS, Mendes BCA, Mingroni Netto RC. Further evidence for loss-of-function mutations in the CEACAM16 gene causing nonsyndromic autosomal recessive hearing loss in humans [Internet]. Journal of Human Genetics. 2019 ; 64 257–260.[citado 2024 set. 28 ] Available from: https://doi.org/10.1038/s10038-018-0546-4

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