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Artigo de periodico
DHFR 19-bp deletion and SHMT C1420T polymorphisms and metabolite concentrations of the folate pathway in individuals with Down syndrome (2013)
Mendes, Cristiani Cortez; Raimundo, Aline Maria Zanchetta de Aquino; Oliveira, Luciana Dutra; Zampieri, Bruna Lancia; Marucci, Gustavo Henrique; Biselli, Joice Matos; Goloni-Bertollo, Eny Maria; Eberlin, Marcos Nogueira; Haddad, Renato; Riccio, Maria Francesca; Vannucchi, Hélio; Carvalho, Valdemir Melechco; Pavarino, Érika Cristina
Fonte: Genetic Testing and Molecular Biomarkers. Unidade: FMRP
Assuntos: SÍNDROME DE DOWN, POLIMORFISMO, EXPRESSÃO GÊNICA, ÁCIDO FÓLICO (METABOLISMO)
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ABNT
MENDES, Cristiani Cortez et al. DHFR 19-bp deletion and SHMT C1420T polymorphisms and metabolite concentrations of the folate pathway in individuals with Down syndrome. Genetic Testing and Molecular Biomarkers, v. 17, n. 4, p. 274-277, 2013Tradução . . Disponível em: https://doi.org/10.1089/gtmb.2012.0293. Acesso em: 22 out. 2025.
APA
Mendes, C. C., Raimundo, A. M. Z. de A., Oliveira, L. D., Zampieri, B. L., Marucci, G. H., Biselli, J. M., et al. (2013). DHFR 19-bp deletion and SHMT C1420T polymorphisms and metabolite concentrations of the folate pathway in individuals with Down syndrome. Genetic Testing and Molecular Biomarkers, 17( 4), 274-277. doi:10.1089/gtmb.2012.0293
NLM
Mendes CC, Raimundo AMZ de A, Oliveira LD, Zampieri BL, Marucci GH, Biselli JM, Goloni-Bertollo EM, Eberlin MN, Haddad R, Riccio MF, Vannucchi H, Carvalho VM, Pavarino ÉC. DHFR 19-bp deletion and SHMT C1420T polymorphisms and metabolite concentrations of the folate pathway in individuals with Down syndrome [Internet]. Genetic Testing and Molecular Biomarkers. 2013 ; 17( 4): 274-277.[citado 2025 out. 22 ] Available from: https://doi.org/10.1089/gtmb.2012.0293
Vancouver
Mendes CC, Raimundo AMZ de A, Oliveira LD, Zampieri BL, Marucci GH, Biselli JM, Goloni-Bertollo EM, Eberlin MN, Haddad R, Riccio MF, Vannucchi H, Carvalho VM, Pavarino ÉC. DHFR 19-bp deletion and SHMT C1420T polymorphisms and metabolite concentrations of the folate pathway in individuals with Down syndrome [Internet]. Genetic Testing and Molecular Biomarkers. 2013 ; 17( 4): 274-277.[citado 2025 out. 22 ] Available from: https://doi.org/10.1089/gtmb.2012.0293
Artigo de periodico
PTPN11 and KRAS Gene Analysis in Patients with Noonan and Noonan-Like Syndromes (2010)
Brasil, Amanda Salem; Pereira, Alexandre C.; Wanderley, Luciana Turolla; Kim, Chong Ae; Malaquias, Alexsandra C.; Jorge, Alexander A. L.; Krieger, José Eduardo; Bertola, Débora Romeo
Fonte: Genetic Testing and Molecular Biomarkers. Unidade: FM
Assuntos: GENES (ANÁLISE), ONCOGENESES, RAQUITISMO, PESOS E MEDIDAS CORPORAIS, PULMÃO (FISIOPATOLOGIA), PESO-ESTATURA
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ABNT
BRASIL, Amanda Salem et al. PTPN11 and KRAS Gene Analysis in Patients with Noonan and Noonan-Like Syndromes. Genetic Testing and Molecular Biomarkers, v. 14, n. 3, p. 425-432, 2010Tradução . . Disponível em: https://doi.org/10.1089/gtmb.2009.0192. Acesso em: 22 out. 2025.
APA
Brasil, A. S., Pereira, A. C., Wanderley, L. T., Kim, C. A., Malaquias, A. C., Jorge, A. A. L., et al. (2010). PTPN11 and KRAS Gene Analysis in Patients with Noonan and Noonan-Like Syndromes. Genetic Testing and Molecular Biomarkers, 14( 3), 425-432. doi:10.1089/gtmb.2009.0192
NLM
Brasil AS, Pereira AC, Wanderley LT, Kim CA, Malaquias AC, Jorge AAL, Krieger JE, Bertola DR. PTPN11 and KRAS Gene Analysis in Patients with Noonan and Noonan-Like Syndromes [Internet]. Genetic Testing and Molecular Biomarkers. 2010 ; 14( 3): 425-432.[citado 2025 out. 22 ] Available from: https://doi.org/10.1089/gtmb.2009.0192
Vancouver
Brasil AS, Pereira AC, Wanderley LT, Kim CA, Malaquias AC, Jorge AAL, Krieger JE, Bertola DR. PTPN11 and KRAS Gene Analysis in Patients with Noonan and Noonan-Like Syndromes [Internet]. Genetic Testing and Molecular Biomarkers. 2010 ; 14( 3): 425-432.[citado 2025 out. 22 ] Available from: https://doi.org/10.1089/gtmb.2009.0192
Artigo de periodico
Role of the mitochondrial mutations, m.827A>G and the novel m.7462C>T, in the origin of hearing loss (2010)
Uehara, Daniela Tiaki; Rincon, Daniel; Abreu-Silva, Ronaldo Serafim; Auricchio, Maria Teresa Ballester de Melo; Tabith Junior, Alfredo; Kok, Fernando; Mingroni Netto, Regina Celia
Fonte: Genetic Testing and Molecular Biomarkers. Unidade: IB
Assuntos: GENÉTICA MÉDICA, PERDA AUDITIVA
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ABNT
UEHARA, Daniela Tiaki et al. Role of the mitochondrial mutations, m.827A>G and the novel m.7462C>T, in the origin of hearing loss. Genetic Testing and Molecular Biomarkers, v. 14, n. 5, p. 611-616, 2010Tradução . . Disponível em: https://doi.org/10.1089/gtmb.2010.0011. Acesso em: 22 out. 2025.
APA
Uehara, D. T., Rincon, D., Abreu-Silva, R. S., Auricchio, M. T. B. de M., Tabith Junior, A., Kok, F., & Mingroni Netto, R. C. (2010). Role of the mitochondrial mutations, m.827A>G and the novel m.7462C>T, in the origin of hearing loss. Genetic Testing and Molecular Biomarkers, 14( 5), 611-616. doi:10.1089/gtmb.2010.0011
NLM
Uehara DT, Rincon D, Abreu-Silva RS, Auricchio MTB de M, Tabith Junior A, Kok F, Mingroni Netto RC. Role of the mitochondrial mutations, m.827A>G and the novel m.7462C>T, in the origin of hearing loss [Internet]. Genetic Testing and Molecular Biomarkers. 2010 ; 14( 5): 611-616.[citado 2025 out. 22 ] Available from: https://doi.org/10.1089/gtmb.2010.0011
Vancouver
Uehara DT, Rincon D, Abreu-Silva RS, Auricchio MTB de M, Tabith Junior A, Kok F, Mingroni Netto RC. Role of the mitochondrial mutations, m.827A>G and the novel m.7462C>T, in the origin of hearing loss [Internet]. Genetic Testing and Molecular Biomarkers. 2010 ; 14( 5): 611-616.[citado 2025 out. 22 ] Available from: https://doi.org/10.1089/gtmb.2010.0011
Artigo de periodico
Williams-Beuren Syndrome: Diagnosis by Polymorphic Markers (2010)
Sbruzzi, Ivanete C.; Pereira, Alexandre C.; Vasconcelos, Beatriz; Honjo, Raquel S.; Krieger, José Eduardo; Kim, Chong A.
Fonte: Genetic Testing and Molecular Biomarkers. Unidade: FM
Assuntos: DELEÇÃO DE GENES, BIOMARCADORES, ELASTINA, FATORES DE RISCO
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ABNT
SBRUZZI, Ivanete C. et al. Williams-Beuren Syndrome: Diagnosis by Polymorphic Markers. Genetic Testing and Molecular Biomarkers, v. 14, n. 2, p. 209-214, 2010Tradução . . Disponível em: https://doi.org/10.1089/gtmb.2009.0120. Acesso em: 22 out. 2025.
APA
Sbruzzi, I. C., Pereira, A. C., Vasconcelos, B., Honjo, R. S., Krieger, J. E., & Kim, C. A. (2010). Williams-Beuren Syndrome: Diagnosis by Polymorphic Markers. Genetic Testing and Molecular Biomarkers, 14( 2), 209-214. doi:10.1089/gtmb.2009.0120
NLM
Sbruzzi IC, Pereira AC, Vasconcelos B, Honjo RS, Krieger JE, Kim CA. Williams-Beuren Syndrome: Diagnosis by Polymorphic Markers [Internet]. Genetic Testing and Molecular Biomarkers. 2010 ; 14( 2): 209-214.[citado 2025 out. 22 ] Available from: https://doi.org/10.1089/gtmb.2009.0120
Vancouver
Sbruzzi IC, Pereira AC, Vasconcelos B, Honjo RS, Krieger JE, Kim CA. Williams-Beuren Syndrome: Diagnosis by Polymorphic Markers [Internet]. Genetic Testing and Molecular Biomarkers. 2010 ; 14( 2): 209-214.[citado 2025 out. 22 ] Available from: https://doi.org/10.1089/gtmb.2009.0120
Artigo de periodico
Hemojuvelin and hepcidin genes sequencing in Brazilian patients with primary iron overload (2010)
Santos, Paulo Caleb Júnior de Lima; Pereira, Alexandre Costa; Cançado, Rodolfo Delfini; Schettert, Isolmar Tadeu; Hirata, Rosario Dominguez Crespo ; Hirata, Mario Hiroyuki ; Figueiredo, Maria Stella; Chiattone, Carlos Sérgio; Krieger, José Eduardo; Guerra-Shinohara, Elvira Maria
Fonte: Genetic Testing and Molecular Biomarkers. Unidades: FCF, FM
Assuntos: SEQUENCIAMENTO GENÉTICO, HEMOCROMATOSE
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ABNT
SANTOS, Paulo Caleb Júnior de Lima et al. Hemojuvelin and hepcidin genes sequencing in Brazilian patients with primary iron overload. Genetic Testing and Molecular Biomarkers, v. 14, n. 6, p. 1-4, 2010Tradução . . Disponível em: https://doi.org/10.1089/gtmb.2010.0056. Acesso em: 22 out. 2025.
APA
Santos, P. C. J. de L., Pereira, A. C., Cançado, R. D., Schettert, I. T., Hirata, R. D. C., Hirata, M. H., et al. (2010). Hemojuvelin and hepcidin genes sequencing in Brazilian patients with primary iron overload. Genetic Testing and Molecular Biomarkers, 14( 6), 1-4. doi:10.1089/gtmb.2010.0056
NLM
Santos PCJ de L, Pereira AC, Cançado RD, Schettert IT, Hirata RDC, Hirata MH, Figueiredo MS, Chiattone CS, Krieger JE, Guerra-Shinohara EM. Hemojuvelin and hepcidin genes sequencing in Brazilian patients with primary iron overload [Internet]. Genetic Testing and Molecular Biomarkers. 2010 ; 14( 6): 1-4.[citado 2025 out. 22 ] Available from: https://doi.org/10.1089/gtmb.2010.0056
Vancouver
Santos PCJ de L, Pereira AC, Cançado RD, Schettert IT, Hirata RDC, Hirata MH, Figueiredo MS, Chiattone CS, Krieger JE, Guerra-Shinohara EM. Hemojuvelin and hepcidin genes sequencing in Brazilian patients with primary iron overload [Internet]. Genetic Testing and Molecular Biomarkers. 2010 ; 14( 6): 1-4.[citado 2025 out. 22 ] Available from: https://doi.org/10.1089/gtmb.2010.0056
Artigo de periodico
Detection of the TLR4 1196C>T polymorphism by mismatched-polymerase chain reaction using plasmid DNA as internal control in restriction fragment length polymorphism assays (2009)
Lima Neto, Lidio Gonçalves; Hirata, Rosario Dominguez Crespo ; Luchessi, André Ducati; Silbiger, Vivian Nogueira; Pastorelli, Carla Prisinzano; Sampaio, Marcelo Ferraz; Armaganijan, Dikran; Rezende, Adriana Augusto de; Doi, Sonia de Quateli; Hirata, Mario Hiroyuki
Fonte: Genetic Testing and Molecular Biomarkers. Unidade: FCF
Assuntos: POLIMORFISMO, REAÇÃO EM CADEIA POR POLIMERASE
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ABNT
LIMA NETO, Lidio Gonçalves et al. Detection of the TLR4 1196C>T polymorphism by mismatched-polymerase chain reaction using plasmid DNA as internal control in restriction fragment length polymorphism assays. Genetic Testing and Molecular Biomarkers, v. 13, n. 3, p. 343-347, 2009Tradução . . Disponível em: http://www.liebertonline.com/doi/pdfplus/10.1089/gtmb.2008.0147. Acesso em: 22 out. 2025.
APA
Lima Neto, L. G., Hirata, R. D. C., Luchessi, A. D., Silbiger, V. N., Pastorelli, C. P., Sampaio, M. F., et al. (2009). Detection of the TLR4 1196C>T polymorphism by mismatched-polymerase chain reaction using plasmid DNA as internal control in restriction fragment length polymorphism assays. Genetic Testing and Molecular Biomarkers, 13( 3), 343-347. Recuperado de http://www.liebertonline.com/doi/pdfplus/10.1089/gtmb.2008.0147
NLM
Lima Neto LG, Hirata RDC, Luchessi AD, Silbiger VN, Pastorelli CP, Sampaio MF, Armaganijan D, Rezende AA de, Doi S de Q, Hirata MH. Detection of the TLR4 1196C>T polymorphism by mismatched-polymerase chain reaction using plasmid DNA as internal control in restriction fragment length polymorphism assays [Internet]. Genetic Testing and Molecular Biomarkers. 2009 ; 13( 3): 343-347.[citado 2025 out. 22 ] Available from: http://www.liebertonline.com/doi/pdfplus/10.1089/gtmb.2008.0147
Vancouver
Lima Neto LG, Hirata RDC, Luchessi AD, Silbiger VN, Pastorelli CP, Sampaio MF, Armaganijan D, Rezende AA de, Doi S de Q, Hirata MH. Detection of the TLR4 1196C>T polymorphism by mismatched-polymerase chain reaction using plasmid DNA as internal control in restriction fragment length polymorphism assays [Internet]. Genetic Testing and Molecular Biomarkers. 2009 ; 13( 3): 343-347.[citado 2025 out. 22 ] Available from: http://www.liebertonline.com/doi/pdfplus/10.1089/gtmb.2008.0147
Artigo de periodico
A Duplex Allele-Specific Amplification PCR to Detect SMN1 Deletion (2009)
Pieri, Patrícia de Campos; Nogueira, Jeronimo de Alencar; Marques-Dias, Maria Joaquina; Resende, Bernadete; Kim, Chong Ae; Reed, Umbertina Conti; Okay, Thelma Suely
Fonte: Genetic Testing and Molecular Biomarkers. Unidade: FM
Assuntos: DOENÇAS NEUROMUSCULARES (GENÉTICA), REAÇÃO EM CADEIA POR POLIMERASE, DELEÇÃO DE GENES, AMPLIFICAÇÃO DE GENES, POLIMORFISMO
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ABNT
PIERI, Patrícia de Campos et al. A Duplex Allele-Specific Amplification PCR to Detect SMN1 Deletion. Genetic Testing and Molecular Biomarkers, v. 13, n. 2, p. 205-208, 2009Tradução . . Disponível em: https://doi.org/10.1089=gtmb.2008.0066. Acesso em: 22 out. 2025.
APA
Pieri, P. de C., Nogueira, J. de A., Marques-Dias, M. J., Resende, B., Kim, C. A., Reed, U. C., & Okay, T. S. (2009). A Duplex Allele-Specific Amplification PCR to Detect SMN1 Deletion. Genetic Testing and Molecular Biomarkers, 13( 2), 205-208. doi:10.1089=gtmb.2008.0066
NLM
Pieri P de C, Nogueira J de A, Marques-Dias MJ, Resende B, Kim CA, Reed UC, Okay TS. A Duplex Allele-Specific Amplification PCR to Detect SMN1 Deletion [Internet]. Genetic Testing and Molecular Biomarkers. 2009 ; 13( 2): 205-208.[citado 2025 out. 22 ] Available from: https://doi.org/10.1089=gtmb.2008.0066
Vancouver
Pieri P de C, Nogueira J de A, Marques-Dias MJ, Resende B, Kim CA, Reed UC, Okay TS. A Duplex Allele-Specific Amplification PCR to Detect SMN1 Deletion [Internet]. Genetic Testing and Molecular Biomarkers. 2009 ; 13( 2): 205-208.[citado 2025 out. 22 ] Available from: https://doi.org/10.1089=gtmb.2008.0066

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