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Artigo de periodico
Ancestry informative marker panel to estimate population stratification using genome-wide human array (2017)
Barbosa, Fernanda B.; Cagnin, Natalia F.; Simioni, Milena; Farias, Allysson A.; Torres, Fábio R.; Molck, Miriam C.; Araujo, Tânia K.; Gil-Da-Silva-Lopes, Vera L.; Donadi, Eduardo Antônio; Simões, Aguinaldo Luiz
Fonte: Annals of Human Genetics. Unidade: FMRP
Assuntos: GENOMAS, ESTRATIFICAÇÃO SOCIAL, POPULAÇÃO, LÚPUS ERITEMATOSO SISTÊMICO
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ABNT
BARBOSA, Fernanda B. et al. Ancestry informative marker panel to estimate population stratification using genome-wide human array. Annals of Human Genetics, v. 81, n. 6, p. 225-233, 2017Tradução . . Disponível em: https://doi.org/10.1111/ahg.12208. Acesso em: 23 out. 2025.
APA
Barbosa, F. B., Cagnin, N. F., Simioni, M., Farias, A. A., Torres, F. R., Molck, M. C., et al. (2017). Ancestry informative marker panel to estimate population stratification using genome-wide human array. Annals of Human Genetics, 81( 6), 225-233. doi:10.1111/ahg.12208
NLM
Barbosa FB, Cagnin NF, Simioni M, Farias AA, Torres FR, Molck MC, Araujo TK, Gil-Da-Silva-Lopes VL, Donadi EA, Simões AL. Ancestry informative marker panel to estimate population stratification using genome-wide human array [Internet]. Annals of Human Genetics. 2017 ; 81( 6): 225-233.[citado 2025 out. 23 ] Available from: https://doi.org/10.1111/ahg.12208
Vancouver
Barbosa FB, Cagnin NF, Simioni M, Farias AA, Torres FR, Molck MC, Araujo TK, Gil-Da-Silva-Lopes VL, Donadi EA, Simões AL. Ancestry informative marker panel to estimate population stratification using genome-wide human array [Internet]. Annals of Human Genetics. 2017 ; 81( 6): 225-233.[citado 2025 out. 23 ] Available from: https://doi.org/10.1111/ahg.12208
Artigo de periodico
Genetic obesity risk and attenuation effect of physical fitness in mexican-mestizo population: a case-control study (2017)
Costa-Urrutia, Paula; Abud, Carolina; Franco-Trecu, Valentina; Colistro, Valentina; Rodríguez‐Arellano, Martha Eunice; Vázquez‐Pérez, Joel; Granados, Julio; Seelaender, Marilia
Fonte: Annals of Human Genetics. Unidade: ICB
Assunto: HISTOLOGIA
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COSTA-URRUTIA, Paula et al. Genetic obesity risk and attenuation effect of physical fitness in mexican-mestizo population: a case-control study. Annals of Human Genetics, v. 81, n. 3, p. 106-116, 2017Tradução . . Disponível em: https://doi.org/10.1111/ahg.12190. Acesso em: 23 out. 2025.
APA
Costa-Urrutia, P., Abud, C., Franco-Trecu, V., Colistro, V., Rodríguez‐Arellano, M. E., Vázquez‐Pérez, J., et al. (2017). Genetic obesity risk and attenuation effect of physical fitness in mexican-mestizo population: a case-control study. Annals of Human Genetics, 81( 3), 106-116. doi:10.1111/ahg.12190
NLM
Costa-Urrutia P, Abud C, Franco-Trecu V, Colistro V, Rodríguez‐Arellano ME, Vázquez‐Pérez J, Granados J, Seelaender M. Genetic obesity risk and attenuation effect of physical fitness in mexican-mestizo population: a case-control study [Internet]. Annals of Human Genetics. 2017 ; 81( 3): 106-116.[citado 2025 out. 23 ] Available from: https://doi.org/10.1111/ahg.12190
Vancouver
Costa-Urrutia P, Abud C, Franco-Trecu V, Colistro V, Rodríguez‐Arellano ME, Vázquez‐Pérez J, Granados J, Seelaender M. Genetic obesity risk and attenuation effect of physical fitness in mexican-mestizo population: a case-control study [Internet]. Annals of Human Genetics. 2017 ; 81( 3): 106-116.[citado 2025 out. 23 ] Available from: https://doi.org/10.1111/ahg.12190
Artigo de periodico
Analysis of circulating miR-1, miR-23a, and miR-26a in atrial fibrillation patients undergoing coronary bypass artery grafting surgery (2017)
Feldman, Andre; Moreira, Dalmo Antonio Ribeiro; Gun, Carlos; Wang, Hui-Tzu Lin; Hirata, Mario Hiroyuki ; Germano, Juliana de Freitas; Leite, Gabriela Guimarães Sousa; Farsky, Pedro
Fonte: Annals of Human Genetics. Unidade: FCF
Assuntos: FIBRILAÇÃO ATRIAL, REVASCULARIZAÇÃO MIOCÁRDICA
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FELDMAN, Andre et al. Analysis of circulating miR-1, miR-23a, and miR-26a in atrial fibrillation patients undergoing coronary bypass artery grafting surgery. Annals of Human Genetics, v. 81, n. 3, p. 99-105, 2017Tradução . . Disponível em: https://doi.org/10.1111/ahg.12188. Acesso em: 23 out. 2025.
APA
Feldman, A., Moreira, D. A. R., Gun, C., Wang, H. -T. L., Hirata, M. H., Germano, J. de F., et al. (2017). Analysis of circulating miR-1, miR-23a, and miR-26a in atrial fibrillation patients undergoing coronary bypass artery grafting surgery. Annals of Human Genetics, 81( 3), 99-105. doi:10.1111/ahg.12188
NLM
Feldman A, Moreira DAR, Gun C, Wang H-TL, Hirata MH, Germano J de F, Leite GGS, Farsky P. Analysis of circulating miR-1, miR-23a, and miR-26a in atrial fibrillation patients undergoing coronary bypass artery grafting surgery [Internet]. Annals of Human Genetics. 2017 ; 81( 3): 99-105.[citado 2025 out. 23 ] Available from: https://doi.org/10.1111/ahg.12188
Vancouver
Feldman A, Moreira DAR, Gun C, Wang H-TL, Hirata MH, Germano J de F, Leite GGS, Farsky P. Analysis of circulating miR-1, miR-23a, and miR-26a in atrial fibrillation patients undergoing coronary bypass artery grafting surgery [Internet]. Annals of Human Genetics. 2017 ; 81( 3): 99-105.[citado 2025 out. 23 ] Available from: https://doi.org/10.1111/ahg.12188
Artigo de periodico
Hydroxymethylbilane Synthase Gene Mutations and Polymorphisms in Brazilian Families with Acute Intermittent Porphyria (2015)
Gonzaga, Ana Denise Gomes; Amorim, Lidia Maria da Fonte de; Fonseca, Ana Beatriz Monteiro; Nogueira, Tatiana Lucia Santos; Pereira, Olga Maria Diniz; Nagai, Maria Aparecida; Barretto, Orlando Cesar de Oliveira; Ribeiro, Georgina Severo
Fonte: Annals of Human Genetics. Unidade: FM
Assuntos: SEQUÊNCIA DO DNA, POPULAÇÃO, MUTAÇÃO GENÉTICA, POLIMORFISMO, REAÇÃO EM CADEIA POR POLIMERASE, BRASIL
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ABNT
GONZAGA, Ana Denise Gomes et al. Hydroxymethylbilane Synthase Gene Mutations and Polymorphisms in Brazilian Families with Acute Intermittent Porphyria. Annals of Human Genetics, v. 79, n. 3, p. 162-172, 2015Tradução . . Disponível em: http://onlinelibrary.wiley.com/doi/10.1111/ahg.12102/epdf. Acesso em: 23 out. 2025.
APA
Gonzaga, A. D. G., Amorim, L. M. da F. de, Fonseca, A. B. M., Nogueira, T. L. S., Pereira, O. M. D., Nagai, M. A., et al. (2015). Hydroxymethylbilane Synthase Gene Mutations and Polymorphisms in Brazilian Families with Acute Intermittent Porphyria. Annals of Human Genetics, 79( 3), 162-172. doi:10.1111/ahg.12102
NLM
Gonzaga ADG, Amorim LM da F de, Fonseca ABM, Nogueira TLS, Pereira OMD, Nagai MA, Barretto OC de O, Ribeiro GS. Hydroxymethylbilane Synthase Gene Mutations and Polymorphisms in Brazilian Families with Acute Intermittent Porphyria [Internet]. Annals of Human Genetics. 2015 ; 79( 3): 162-172.[citado 2025 out. 23 ] Available from: http://onlinelibrary.wiley.com/doi/10.1111/ahg.12102/epdf
Vancouver
Gonzaga ADG, Amorim LM da F de, Fonseca ABM, Nogueira TLS, Pereira OMD, Nagai MA, Barretto OC de O, Ribeiro GS. Hydroxymethylbilane Synthase Gene Mutations and Polymorphisms in Brazilian Families with Acute Intermittent Porphyria [Internet]. Annals of Human Genetics. 2015 ; 79( 3): 162-172.[citado 2025 out. 23 ] Available from: http://onlinelibrary.wiley.com/doi/10.1111/ahg.12102/epdf
Artigo de periodico
Spastic paraplegia, optic atrophy, and neuropathy: new observations, Locus Refinement, and Exclusion of candidate genes (2009)
Macedo-Souza, Lúcia Inês; Kok, Fernando; Santos, Silvana; Licinio, Luciana; Lezirovitz, Karina; Cavaçana, Natale; Bueno, Clarissa; Amorim, Simone; Pessoa, André; Graciani, Zodja; Ferreira, Áurea Fávero; Prazeres, Abdísio; Melo, Aurea Nogueira de; Otto, Paulo A ; Zatz, Mayana
Fonte: Annals of Human Genetics. Unidade: IB
Assuntos: DOENÇAS NEURODEGENERATIVAS, GENÉTICA MÉDICA
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ABNT
MACEDO-SOUZA, Lúcia Inês et al. Spastic paraplegia, optic atrophy, and neuropathy: new observations, Locus Refinement, and Exclusion of candidate genes. Annals of Human Genetics, v. 73, n. 3, p. 382-387, 2009Tradução . . Disponível em: https://doi.org/10.1111/j.1469-1809.2009.00507.x. Acesso em: 23 out. 2025.
APA
Macedo-Souza, L. I., Kok, F., Santos, S., Licinio, L., Lezirovitz, K., Cavaçana, N., et al. (2009). Spastic paraplegia, optic atrophy, and neuropathy: new observations, Locus Refinement, and Exclusion of candidate genes. Annals of Human Genetics, 73( 3), 382-387. doi:10.1111/j.1469-1809.2009.00507.x
NLM
Macedo-Souza LI, Kok F, Santos S, Licinio L, Lezirovitz K, Cavaçana N, Bueno C, Amorim S, Pessoa A, Graciani Z, Ferreira ÁF, Prazeres A, Melo AN de, Otto PA, Zatz M. Spastic paraplegia, optic atrophy, and neuropathy: new observations, Locus Refinement, and Exclusion of candidate genes [Internet]. Annals of Human Genetics. 2009 ; 73( 3): 382-387.[citado 2025 out. 23 ] Available from: https://doi.org/10.1111/j.1469-1809.2009.00507.x
Vancouver
Macedo-Souza LI, Kok F, Santos S, Licinio L, Lezirovitz K, Cavaçana N, Bueno C, Amorim S, Pessoa A, Graciani Z, Ferreira ÁF, Prazeres A, Melo AN de, Otto PA, Zatz M. Spastic paraplegia, optic atrophy, and neuropathy: new observations, Locus Refinement, and Exclusion of candidate genes [Internet]. Annals of Human Genetics. 2009 ; 73( 3): 382-387.[citado 2025 out. 23 ] Available from: https://doi.org/10.1111/j.1469-1809.2009.00507.x
Artigo de periodico
Multiplique founder haplotypes of mitochondrial DNA in Ameridians revealed by RFLP and sequencing (1996)
Santos, Sidney Emanuel Batista dos; Ribeiro-dos-Santos, Andrea K. C.; Meyer, Daniel; Zago, Marco Antônio
Fonte: Annals of Human Genetics. Unidade: FMRP
Assuntos: GENÉTICA MÉDICA, MITOCÔNDRIAS, DNA
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ABNT
SANTOS, Sidney Emanuel Batista dos et al. Multiplique founder haplotypes of mitochondrial DNA in Ameridians revealed by RFLP and sequencing. Annals of Human Genetics, v. 60, p. 305-319, 1996Tradução . . Disponível em: https://doi.org/10.1111/j.1469-1809.1996.tb01194.x. Acesso em: 23 out. 2025.
APA
Santos, S. E. B. dos, Ribeiro-dos-Santos, A. K. C., Meyer, D., & Zago, M. A. (1996). Multiplique founder haplotypes of mitochondrial DNA in Ameridians revealed by RFLP and sequencing. Annals of Human Genetics, 60, 305-319. doi:10.1111/j.1469-1809.1996.tb01194.x
NLM
Santos SEB dos, Ribeiro-dos-Santos AKC, Meyer D, Zago MA. Multiplique founder haplotypes of mitochondrial DNA in Ameridians revealed by RFLP and sequencing [Internet]. Annals of Human Genetics. 1996 ; 60 305-319.[citado 2025 out. 23 ] Available from: https://doi.org/10.1111/j.1469-1809.1996.tb01194.x
Vancouver
Santos SEB dos, Ribeiro-dos-Santos AKC, Meyer D, Zago MA. Multiplique founder haplotypes of mitochondrial DNA in Ameridians revealed by RFLP and sequencing [Internet]. Annals of Human Genetics. 1996 ; 60 305-319.[citado 2025 out. 23 ] Available from: https://doi.org/10.1111/j.1469-1809.1996.tb01194.x
Artigo de periodico
Racial heterogeneity of dna polymorphisms linked to the a and o alleles of the abo blood group gene (1996)
Zago, M A; Tavella, M H; Simoes, B P; Franco, R F; Guerreiro, J F; Santos, S B
Fonte: Annals of Human Genetics. Unidade: FMRP
Assunto: GENÉTICA
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ABNT
ZAGO, M A et al. Racial heterogeneity of dna polymorphisms linked to the a and o alleles of the abo blood group gene. Annals of Human Genetics, v. 60, p. 67-72, 1996Tradução . . Acesso em: 23 out. 2025.
APA
Zago, M. A., Tavella, M. H., Simoes, B. P., Franco, R. F., Guerreiro, J. F., & Santos, S. B. (1996). Racial heterogeneity of dna polymorphisms linked to the a and o alleles of the abo blood group gene. Annals of Human Genetics, 60, 67-72.
NLM
Zago MA, Tavella MH, Simoes BP, Franco RF, Guerreiro JF, Santos SB. Racial heterogeneity of dna polymorphisms linked to the a and o alleles of the abo blood group gene. Annals of Human Genetics. 1996 ;60 67-72.[citado 2025 out. 23 ]
Vancouver
Zago MA, Tavella MH, Simoes BP, Franco RF, Guerreiro JF, Santos SB. Racial heterogeneity of dna polymorphisms linked to the a and o alleles of the abo blood group gene. Annals of Human Genetics. 1996 ;60 67-72.[citado 2025 out. 23 ]
Artigo de periodico
Rflp map for 2q33-q37 from multicase mycobacterial and leishmanial disease families: no evidence for an lsh / ity / bcb gene homologue influencing susceptibility in leprosy (1993)
Shaw, M A; Atkinson, S; Dockerall, H; Hussain, R; Lins Lainson, Z; Shaw, Jeffrey Jon; Ramos, F; Silveira, F; Mehdi, S Q; Kaukab, F; Kahliq, S; Chiang, T
Fonte: Annals of Human Genetics. Unidade: ICB
Assunto: PARASITOLOGIA
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ABNT
SHAW, M A et al. Rflp map for 2q33-q37 from multicase mycobacterial and leishmanial disease families: no evidence for an lsh / ity / bcb gene homologue influencing susceptibility in leprosy. Annals of Human Genetics, v. 57, n. 4 , p. 251-71, 1993Tradução . . Acesso em: 23 out. 2025.
APA
Shaw, M. A., Atkinson, S., Dockerall, H., Hussain, R., Lins Lainson, Z., Shaw, J. J., et al. (1993). Rflp map for 2q33-q37 from multicase mycobacterial and leishmanial disease families: no evidence for an lsh / ity / bcb gene homologue influencing susceptibility in leprosy. Annals of Human Genetics, 57( 4 ), 251-71.
NLM
Shaw MA, Atkinson S, Dockerall H, Hussain R, Lins Lainson Z, Shaw JJ, Ramos F, Silveira F, Mehdi SQ, Kaukab F, Kahliq S, Chiang T. Rflp map for 2q33-q37 from multicase mycobacterial and leishmanial disease families: no evidence for an lsh / ity / bcb gene homologue influencing susceptibility in leprosy. Annals of Human Genetics. 1993 ;57( 4 ): 251-71.[citado 2025 out. 23 ]
Vancouver
Shaw MA, Atkinson S, Dockerall H, Hussain R, Lins Lainson Z, Shaw JJ, Ramos F, Silveira F, Mehdi SQ, Kaukab F, Kahliq S, Chiang T. Rflp map for 2q33-q37 from multicase mycobacterial and leishmanial disease families: no evidence for an lsh / ity / bcb gene homologue influencing susceptibility in leprosy. Annals of Human Genetics. 1993 ;57( 4 ): 251-71.[citado 2025 out. 23 ]
Artigo de periodico
The rate of spontaneous sex-linked mutations and the doubling dose in man (1960)
Frota-Pessoa, Oswaldo; Saldanha, Pedro Henrique
Fonte: Annals of Human Genetics. Unidade: IB
Assunto: MUTAÇÃO GENÉTICA
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ABNT
FROTA-PESSOA, Oswaldo e SALDANHA, Pedro Henrique. The rate of spontaneous sex-linked mutations and the doubling dose in man. Annals of Human Genetics, v. 24, p. 367-373, 1960Tradução . . Disponível em: https://doi.org/10.1111/j.1469-1809.1960.tb01749.x. Acesso em: 23 out. 2025.
APA
Frota-Pessoa, O., & Saldanha, P. H. (1960). The rate of spontaneous sex-linked mutations and the doubling dose in man. Annals of Human Genetics, 24, 367-373. doi:10.1111/j.1469-1809.1960.tb01749.x
NLM
Frota-Pessoa O, Saldanha PH. The rate of spontaneous sex-linked mutations and the doubling dose in man [Internet]. Annals of Human Genetics. 1960 ; 24 367-373.[citado 2025 out. 23 ] Available from: https://doi.org/10.1111/j.1469-1809.1960.tb01749.x
Vancouver
Frota-Pessoa O, Saldanha PH. The rate of spontaneous sex-linked mutations and the doubling dose in man [Internet]. Annals of Human Genetics. 1960 ; 24 367-373.[citado 2025 out. 23 ] Available from: https://doi.org/10.1111/j.1469-1809.1960.tb01749.x

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