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Artigo de periodico
Increased prevalence of the null allele of the p.Arg577Ter variant in the ACTN3 gene in Brazilian long-distance athletes: A retrospective study (2024)
Guilherme, João Paulo Limongi França ; Oliveira, Edilamar Menezes de
Source: Annals of human genetics. Unidade: EEFE
Subjects: DESEMPENHO ESPORTIVO, GENÓTIPOS, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUILHERME, João Paulo Limongi França e OLIVEIRA, Edilamar Menezes de. Increased prevalence of the null allele of the p.Arg577Ter variant in the ACTN3 gene in Brazilian long-distance athletes: A retrospective study. Annals of human genetics, v. 88, p. 414-422, 2024Tradução . . Disponível em: https://doi.org/10.1111/ahg.12571. Acesso em: 25 abr. 2026.
APA
Guilherme, J. P. L. F., & Oliveira, E. M. de. (2024). Increased prevalence of the null allele of the p.Arg577Ter variant in the ACTN3 gene in Brazilian long-distance athletes: A retrospective study. Annals of human genetics, 88, 414-422. doi:10.1111/ahg.12571
NLM
Guilherme JPLF, Oliveira EM de. Increased prevalence of the null allele of the p.Arg577Ter variant in the ACTN3 gene in Brazilian long-distance athletes: A retrospective study [Internet]. Annals of human genetics. 2024 ; 88 414-422.[citado 2026 abr. 25 ] Available from: https://doi.org/10.1111/ahg.12571
Vancouver
Guilherme JPLF, Oliveira EM de. Increased prevalence of the null allele of the p.Arg577Ter variant in the ACTN3 gene in Brazilian long-distance athletes: A retrospective study [Internet]. Annals of human genetics. 2024 ; 88 414-422.[citado 2026 abr. 25 ] Available from: https://doi.org/10.1111/ahg.12571
Artigo de periodico
Detection of mosaicism for segmental and whole chromosome imbalances by targeted sequencing (2021)
Villela, Darine; Barros, Juliana Sobral de; Costa, Silvia Souza da; Aguiar, Talita F. M; Campagnari, Francine; Vianna-Morgante, Angela M ; Krepischi, Ana Cristina Victorino ; Rosenberg, Carla
Source: Annals of human genetics. Unidade: IB
Subjects: GENOMAS, ANORMALIDADES CROMOSSÔMICAS, SEQUÊNCIA DO DNA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VILLELA, Darine et al. Detection of mosaicism for segmental and whole chromosome imbalances by targeted sequencing. Annals of human genetics, v. 85, n. Ja 2021, p. 18-26, 2021Tradução . . Disponível em: https://doi.org/10.1111/ahg.12402. Acesso em: 25 abr. 2026.
APA
Villela, D., Barros, J. S. de, Costa, S. S. da, Aguiar, T. F. M., Campagnari, F., Vianna-Morgante, A. M., et al. (2021). Detection of mosaicism for segmental and whole chromosome imbalances by targeted sequencing. Annals of human genetics, 85( Ja 2021), 18-26. doi:10.1111/ahg.12402
NLM
Villela D, Barros JS de, Costa SS da, Aguiar TFM, Campagnari F, Vianna-Morgante AM, Krepischi ACV, Rosenberg C. Detection of mosaicism for segmental and whole chromosome imbalances by targeted sequencing [Internet]. Annals of human genetics. 2021 ; 85( Ja 2021): 18-26.[citado 2026 abr. 25 ] Available from: https://doi.org/10.1111/ahg.12402
Vancouver
Villela D, Barros JS de, Costa SS da, Aguiar TFM, Campagnari F, Vianna-Morgante AM, Krepischi ACV, Rosenberg C. Detection of mosaicism for segmental and whole chromosome imbalances by targeted sequencing [Internet]. Annals of human genetics. 2021 ; 85( Ja 2021): 18-26.[citado 2026 abr. 25 ] Available from: https://doi.org/10.1111/ahg.12402
Artigo de periodico
Total genotype score and athletic status: An exploratory cross-sectional study of a Brazilian athlete cohort (2020)
Guilherme, João Paulo Limongi França ; Lancha Junior, Antonio Herbert
Source: Annals of human genetics. Unidade: EEFE
Subjects: POLIMORFISMO, FORÇA MUSCULAR, GENÉTICA, DESEMPENHO ESPORTIVO, ESPORTES, ATLETAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUILHERME, João Paulo Limongi França e LANCHA JUNIOR, Antonio Herbert. Total genotype score and athletic status: An exploratory cross-sectional study of a Brazilian athlete cohort. Annals of human genetics, v. 84, n. 2, p. 141-150, 2020Tradução . . Disponível em: https://doi.org/10.1111/ahg.12353. Acesso em: 25 abr. 2026.
APA
Guilherme, J. P. L. F., & Lancha Junior, A. H. (2020). Total genotype score and athletic status: An exploratory cross-sectional study of a Brazilian athlete cohort. Annals of human genetics, 84( 2), 141-150. doi:10.1111/ahg.12353
NLM
Guilherme JPLF, Lancha Junior AH. Total genotype score and athletic status: An exploratory cross-sectional study of a Brazilian athlete cohort [Internet]. Annals of human genetics. 2020 ; 84( 2): 141-150.[citado 2026 abr. 25 ] Available from: https://doi.org/10.1111/ahg.12353
Vancouver
Guilherme JPLF, Lancha Junior AH. Total genotype score and athletic status: An exploratory cross-sectional study of a Brazilian athlete cohort [Internet]. Annals of human genetics. 2020 ; 84( 2): 141-150.[citado 2026 abr. 25 ] Available from: https://doi.org/10.1111/ahg.12353
Artigo de periodico
Analysis of sports-relevant polymorphisms in a large Brazilian cohort of top-level athletes (2018)
Guilherme, João Paulo Limongi França ; Bertuzzi, Rômulo Cássio de Moraes; Pereira, Alexandre da Costa; Lancha Junior, Antonio Herbert
Source: Annals of human genetics. Unidade: EEFE
Subjects: GENÉTICA, POLIMORFISMO, DESEMPENHO ESPORTIVO, BRASIL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUILHERME, João Paulo Limongi França et al. Analysis of sports-relevant polymorphisms in a large Brazilian cohort of top-level athletes. Annals of human genetics, p. 11 , 2018Tradução . . Disponível em: https://doi.org/10.1111/ahg.12248. Acesso em: 25 abr. 2026.
APA
Guilherme, J. P. L. F., Bertuzzi, R. C. de M., Pereira, A. da C., & Lancha Junior, A. H. (2018). Analysis of sports-relevant polymorphisms in a large Brazilian cohort of top-level athletes. Annals of human genetics, 11 . doi:10.1111/ahg.12248
NLM
Guilherme JPLF, Bertuzzi RC de M, Pereira A da C, Lancha Junior AH. Analysis of sports-relevant polymorphisms in a large Brazilian cohort of top-level athletes [Internet]. Annals of human genetics. 2018 ; 11 .[citado 2026 abr. 25 ] Available from: https://doi.org/10.1111/ahg.12248
Vancouver
Guilherme JPLF, Bertuzzi RC de M, Pereira A da C, Lancha Junior AH. Analysis of sports-relevant polymorphisms in a large Brazilian cohort of top-level athletes [Internet]. Annals of human genetics. 2018 ; 11 .[citado 2026 abr. 25 ] Available from: https://doi.org/10.1111/ahg.12248
Artigo de periodico
Exome sequencing identifies a novel nonsense mutation of MYO6 as the cause of deafness in a brazilian family (2018)
Sampaio-silva, Juliana; Bento, Ricardo Ferreira
Source: Annals of human genetics. Unidade: FM
Subjects: SURDEZ, DOENÇAS GENÉTICAS, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SAMPAIO-SILVA, Juliana e BENTO, Ricardo Ferreira. Exome sequencing identifies a novel nonsense mutation of MYO6 as the cause of deafness in a brazilian family. Annals of human genetics, v. 82, n. 1, p. 23-34, 2018Tradução . . Disponível em: https://doi.org/10.1111/ahg.12213. Acesso em: 25 abr. 2026.
APA
Sampaio-silva, J., & Bento, R. F. (2018). Exome sequencing identifies a novel nonsense mutation of MYO6 as the cause of deafness in a brazilian family. Annals of human genetics, 82( 1), 23-34. doi:10.1111/ahg.12213
NLM
Sampaio-silva J, Bento RF. Exome sequencing identifies a novel nonsense mutation of MYO6 as the cause of deafness in a brazilian family [Internet]. Annals of human genetics. 2018 ; 82( 1): 23-34.[citado 2026 abr. 25 ] Available from: https://doi.org/10.1111/ahg.12213
Vancouver
Sampaio-silva J, Bento RF. Exome sequencing identifies a novel nonsense mutation of MYO6 as the cause of deafness in a brazilian family [Internet]. Annals of human genetics. 2018 ; 82( 1): 23-34.[citado 2026 abr. 25 ] Available from: https://doi.org/10.1111/ahg.12213

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