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Filtros : "FM-MFT" "Genetics and Molecular Research" Removidos: "Indexado no: Science Citation Index Expanded" "DNA MITOCONDRIAL" "Louro, Iúri Drumond" Limpar

Filtros

Artigo de periodico
A genetic linkage study in Brazil identifies a new locus for persistent developmental stuttering on chromosome 10 (2014)
Domingues, C. E. F.; Oliveira, C. M. C.; Oliveira, B. V.; Juste, F. S.; Andrade, C. R. F.; Giancheti, C. M.; Moretti-Ferreira, D.; Drayana, D.
Source: Genetics and Molecular Research. Unidade: FM
Subjects: GAGUEIRA, CROMOSSOMOS, EXPRESSÃO GÊNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DOMINGUES, C. E. F. et al. A genetic linkage study in Brazil identifies a new locus for persistent developmental stuttering on chromosome 10. Genetics and Molecular Research, v. 13, n. 1, p. 2094-2101, 2014Tradução . . Disponível em: https://doi.org/10.4238/2014.March.24.13. Acesso em: 18 nov. 2024.
APA
Domingues, C. E. F., Oliveira, C. M. C., Oliveira, B. V., Juste, F. S., Andrade, C. R. F., Giancheti, C. M., et al. (2014). A genetic linkage study in Brazil identifies a new locus for persistent developmental stuttering on chromosome 10. Genetics and Molecular Research, 13( 1), 2094-2101. doi:10.4238/2014.March.24.13
NLM
Domingues CEF, Oliveira CMC, Oliveira BV, Juste FS, Andrade CRF, Giancheti CM, Moretti-Ferreira D, Drayana D. A genetic linkage study in Brazil identifies a new locus for persistent developmental stuttering on chromosome 10 [Internet]. Genetics and Molecular Research. 2014 ; 13( 1): 2094-2101.[citado 2024 nov. 18 ] Available from: https://doi.org/10.4238/2014.March.24.13
Vancouver
Domingues CEF, Oliveira CMC, Oliveira BV, Juste FS, Andrade CRF, Giancheti CM, Moretti-Ferreira D, Drayana D. A genetic linkage study in Brazil identifies a new locus for persistent developmental stuttering on chromosome 10 [Internet]. Genetics and Molecular Research. 2014 ; 13( 1): 2094-2101.[citado 2024 nov. 18 ] Available from: https://doi.org/10.4238/2014.March.24.13
Artigo de periodico
Johanson-Blizzard syndrome: a report of gender-discordant twins with a novel UBR1 mutation (2014)
Quaio, C. R.; Koda, Y. K.; Bertola, D. R.; Sukalo, M.; Zenker, M.; Kim, C. A.
Source: Genetics and Molecular Research. Unidades: FM, IB
Subjects: GÊMEOS, EXPRESSÃO GÊNICA, PANCREATOPATIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
QUAIO, C. R. et al. Johanson-Blizzard syndrome: a report of gender-discordant twins with a novel UBR1 mutation. Genetics and Molecular Research, v. 13, n. 2, p. 4159-4164, 2014Tradução . . Disponível em: https://doi.org/10.4238/2014.June.9.2. Acesso em: 18 nov. 2024.
APA
Quaio, C. R., Koda, Y. K., Bertola, D. R., Sukalo, M., Zenker, M., & Kim, C. A. (2014). Johanson-Blizzard syndrome: a report of gender-discordant twins with a novel UBR1 mutation. Genetics and Molecular Research, 13( 2), 4159-4164. doi:10.4238/2014.June.9.2
NLM
Quaio CR, Koda YK, Bertola DR, Sukalo M, Zenker M, Kim CA. Johanson-Blizzard syndrome: a report of gender-discordant twins with a novel UBR1 mutation [Internet]. Genetics and Molecular Research. 2014 ; 13( 2): 4159-4164.[citado 2024 nov. 18 ] Available from: https://doi.org/10.4238/2014.June.9.2
Vancouver
Quaio CR, Koda YK, Bertola DR, Sukalo M, Zenker M, Kim CA. Johanson-Blizzard syndrome: a report of gender-discordant twins with a novel UBR1 mutation [Internet]. Genetics and Molecular Research. 2014 ; 13( 2): 4159-4164.[citado 2024 nov. 18 ] Available from: https://doi.org/10.4238/2014.June.9.2

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