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BRANDÃO, Paulo Eduardo et al. Emergence of Avian coronavirus escape mutants under suboptimal antibody titers. Journal of Molecular Evolution, v. 90, p. 176-181, 2022Tradução . . Disponível em: https://doi.org/10.1007/s00239-022-10050-8. Acesso em: 11 ago. 2024.
APA
Brandão, P. E., Berg, M., Silva, S. O. de S., & Taniwaki, S. A. (2022). Emergence of Avian coronavirus escape mutants under suboptimal antibody titers. Journal of Molecular Evolution, 90, 176-181. doi:10.1007/s00239-022-10050-8
NLM
Brandão PE, Berg M, Silva SO de S, Taniwaki SA. Emergence of Avian coronavirus escape mutants under suboptimal antibody titers [Internet]. Journal of Molecular Evolution. 2022 ; 90 176-181.[citado 2024 ago. 11 ] Available from: https://doi.org/10.1007/s00239-022-10050-8
Vancouver
Brandão PE, Berg M, Silva SO de S, Taniwaki SA. Emergence of Avian coronavirus escape mutants under suboptimal antibody titers [Internet]. Journal of Molecular Evolution. 2022 ; 90 176-181.[citado 2024 ago. 11 ] Available from: https://doi.org/10.1007/s00239-022-10050-8
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LOPES, Tiago Falcon et al. Exploring integument transcriptomes, cuticle ultrastructure, and cuticular hydrocarbons profiles in eusocial and solitary bee species displaying heterochronic adult cuticle maturation. PLOS ONE, v. 14, n. 3, p. [38] , 2019Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0213796. Acesso em: 11 ago. 2024.
APA
Lopes, T. F., Pinheiro, D. G., Ferreira-Caliman, M. J., Turatti, I. C. C., Abreu, F. C. P. de, Galaschi-Teixeira, J. S., et al. (2019). Exploring integument transcriptomes, cuticle ultrastructure, and cuticular hydrocarbons profiles in eusocial and solitary bee species displaying heterochronic adult cuticle maturation. PLOS ONE, 14( 3), [38] . doi:10.1371/journal.pone.0213796
NLM
Lopes TF, Pinheiro DG, Ferreira-Caliman MJ, Turatti ICC, Abreu FCP de, Galaschi-Teixeira JS, Martins JR, Elias-Neto M, Soares MPM, Laure MAFB, Figueiredo VLC, Lopes NP, Simões ZLP, Garófalo CA, Bitondi MMG. Exploring integument transcriptomes, cuticle ultrastructure, and cuticular hydrocarbons profiles in eusocial and solitary bee species displaying heterochronic adult cuticle maturation [Internet]. PLOS ONE. 2019 ; 14( 3): [38] .[citado 2024 ago. 11 ] Available from: https://doi.org/10.1371/journal.pone.0213796
Vancouver
Lopes TF, Pinheiro DG, Ferreira-Caliman MJ, Turatti ICC, Abreu FCP de, Galaschi-Teixeira JS, Martins JR, Elias-Neto M, Soares MPM, Laure MAFB, Figueiredo VLC, Lopes NP, Simões ZLP, Garófalo CA, Bitondi MMG. Exploring integument transcriptomes, cuticle ultrastructure, and cuticular hydrocarbons profiles in eusocial and solitary bee species displaying heterochronic adult cuticle maturation [Internet]. PLOS ONE. 2019 ; 14( 3): [38] .[citado 2024 ago. 11 ] Available from: https://doi.org/10.1371/journal.pone.0213796
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DANILOVIC, Debora L. S. et al. Pre-operative role of BRAF in the guidance of the surgical approach and prognosis of differentiated thyroid carcinoma. European Journal of Endocrinology, v. 170, n. 4, p. 619-625, 2014Tradução . . Disponível em: https://doi.org/10.1530/EJE-13-0944. Acesso em: 11 ago. 2024.
APA
Danilovic, D. L. S., Lima, E. U., Domingues, R. B., Brandao, L. G., Hoff, A. O., & Marui, S. (2014). Pre-operative role of BRAF in the guidance of the surgical approach and prognosis of differentiated thyroid carcinoma. European Journal of Endocrinology, 170( 4), 619-625. doi:10.1530/EJE-13-0944
NLM
Danilovic DLS, Lima EU, Domingues RB, Brandao LG, Hoff AO, Marui S. Pre-operative role of BRAF in the guidance of the surgical approach and prognosis of differentiated thyroid carcinoma [Internet]. European Journal of Endocrinology. 2014 ; 170( 4): 619-625.[citado 2024 ago. 11 ] Available from: https://doi.org/10.1530/EJE-13-0944
Vancouver
Danilovic DLS, Lima EU, Domingues RB, Brandao LG, Hoff AO, Marui S. Pre-operative role of BRAF in the guidance of the surgical approach and prognosis of differentiated thyroid carcinoma [Internet]. European Journal of Endocrinology. 2014 ; 170( 4): 619-625.[citado 2024 ago. 11 ] Available from: https://doi.org/10.1530/EJE-13-0944
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CARVALHO, Claudia M.B. et al. Dosage Changes of a Segment at 17p13.1 Lead to Intellectual Disability and Microcephaly as a Result of Complex Genetic Interaction of Multiple Genes. American Journal of Human Genetics, v. 95, p. 565-578, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.ajhg.2014.10.006. Acesso em: 11 ago. 2024.
APA
Carvalho, C. M. B., Vasanth, S., Shinawi, M., Russell, C., Ramocki, M. B., Brown, C. W., et al. (2014). Dosage Changes of a Segment at 17p13.1 Lead to Intellectual Disability and Microcephaly as a Result of Complex Genetic Interaction of Multiple Genes. American Journal of Human Genetics, 95, 565-578. doi:10.1016/j.ajhg.2014.10.006
NLM
Carvalho CMB, Vasanth S, Shinawi M, Russell C, Ramocki MB, Brown CW, Graakjaer J, Skytte A-B, Patel GS, Immken LD, Aleck K, Lim C, Cheung SW, Rosenberg C, Katsanis N, Lupski JR. Dosage Changes of a Segment at 17p13.1 Lead to Intellectual Disability and Microcephaly as a Result of Complex Genetic Interaction of Multiple Genes [Internet]. American Journal of Human Genetics. 2014 ; 95 565-578.[citado 2024 ago. 11 ] Available from: https://doi.org/10.1016/j.ajhg.2014.10.006
Vancouver
Carvalho CMB, Vasanth S, Shinawi M, Russell C, Ramocki MB, Brown CW, Graakjaer J, Skytte A-B, Patel GS, Immken LD, Aleck K, Lim C, Cheung SW, Rosenberg C, Katsanis N, Lupski JR. Dosage Changes of a Segment at 17p13.1 Lead to Intellectual Disability and Microcephaly as a Result of Complex Genetic Interaction of Multiple Genes [Internet]. American Journal of Human Genetics. 2014 ; 95 565-578.[citado 2024 ago. 11 ] Available from: https://doi.org/10.1016/j.ajhg.2014.10.006
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SÁ, V. de et al. Epidermal growth factor receptor mutations in primary and metastatic adenocarcinomas from a tertiary hospital in São Paulo, Brazil. Virchows Archiv. Berlin: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1007/s00428-013-1444-y. Acesso em: 11 ago. 2024. , 2013
APA
Sá, V. de, Nascimento, E., Meireles, S., & Capelozzi, V. (2013). Epidermal growth factor receptor mutations in primary and metastatic adenocarcinomas from a tertiary hospital in São Paulo, Brazil. Virchows Archiv. Berlin: Faculdade de Medicina, Universidade de São Paulo. doi:10.1007/s00428-013-1444-y
NLM
Sá V de, Nascimento E, Meireles S, Capelozzi V. Epidermal growth factor receptor mutations in primary and metastatic adenocarcinomas from a tertiary hospital in São Paulo, Brazil [Internet]. Virchows Archiv. 2013 ; 463( 2): 236.[citado 2024 ago. 11 ] Available from: https://doi.org/10.1007/s00428-013-1444-y
Vancouver
Sá V de, Nascimento E, Meireles S, Capelozzi V. Epidermal growth factor receptor mutations in primary and metastatic adenocarcinomas from a tertiary hospital in São Paulo, Brazil [Internet]. Virchows Archiv. 2013 ; 463( 2): 236.[citado 2024 ago. 11 ] Available from: https://doi.org/10.1007/s00428-013-1444-y
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FRAGOSO, Maria Candida B. V. et al. Combined expression of BUB1B, DLG7, and PINK1 as predictors of poor outcome in adrenocortical tumors: validation in a Brazilian cohort of adult and pediatric patients. European Journal of Endocrinology, v. 166, n. 1, p. 61-67, 2012Tradução . . Disponível em: https://doi.org/10.1530/EJE-11-0964. Acesso em: 11 ago. 2024.
APA
Fragoso, M. C. B. V., Almeida, M. Q., Mazzuco, T. L., Mariani, B. M. P., Brito, L. P., Gonçalves, T. C., et al. (2012). Combined expression of BUB1B, DLG7, and PINK1 as predictors of poor outcome in adrenocortical tumors: validation in a Brazilian cohort of adult and pediatric patients. European Journal of Endocrinology, 166( 1), 61-67. doi:10.1530/EJE-11-0964
NLM
Fragoso MCBV, Almeida MQ, Mazzuco TL, Mariani BMP, Brito LP, Gonçalves TC, Alencar GA, Lima L de O, Faria AM, Bourdeau I, Lucon AM, Freire DS, Latronico AC, Mendonca BB, Lacroix A, Lerario AM. Combined expression of BUB1B, DLG7, and PINK1 as predictors of poor outcome in adrenocortical tumors: validation in a Brazilian cohort of adult and pediatric patients [Internet]. European Journal of Endocrinology. 2012 ; 166( 1): 61-67.[citado 2024 ago. 11 ] Available from: https://doi.org/10.1530/EJE-11-0964
Vancouver
Fragoso MCBV, Almeida MQ, Mazzuco TL, Mariani BMP, Brito LP, Gonçalves TC, Alencar GA, Lima L de O, Faria AM, Bourdeau I, Lucon AM, Freire DS, Latronico AC, Mendonca BB, Lacroix A, Lerario AM. Combined expression of BUB1B, DLG7, and PINK1 as predictors of poor outcome in adrenocortical tumors: validation in a Brazilian cohort of adult and pediatric patients [Internet]. European Journal of Endocrinology. 2012 ; 166( 1): 61-67.[citado 2024 ago. 11 ] Available from: https://doi.org/10.1530/EJE-11-0964
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BERTOLA, D. R. et al. Multiple, diffuse schwannomas in a RASopathy phenotype patient with germline KRAS mutation [Carta]: a causal relationship?. Clinical Genetics. Copenhagem: Instituto de Biociências, Universidade de São Paulo. Disponível em: https://doi.org/10.1111/j.1399-0004.2011.01764.x. Acesso em: 11 ago. 2024. , 2012
APA
Bertola, D. R., Pereira, A. C., Brasil, A. S., Suzuki, L., Leite, C., Falzoni, R., et al. (2012). Multiple, diffuse schwannomas in a RASopathy phenotype patient with germline KRAS mutation [Carta]: a causal relationship? Clinical Genetics. Copenhagem: Instituto de Biociências, Universidade de São Paulo. doi:10.1111/j.1399-0004.2011.01764.x
NLM
Bertola DR, Pereira AC, Brasil AS, Suzuki L, Leite C, Falzoni R, Tannuri U, Poplawski AB, Janowski KM, Kim CA, Messiaena LM. Multiple, diffuse schwannomas in a RASopathy phenotype patient with germline KRAS mutation [Carta]: a causal relationship? [Internet]. Clinical Genetics. 2012 ; 81( 6): 595-597.[citado 2024 ago. 11 ] Available from: https://doi.org/10.1111/j.1399-0004.2011.01764.x
Vancouver
Bertola DR, Pereira AC, Brasil AS, Suzuki L, Leite C, Falzoni R, Tannuri U, Poplawski AB, Janowski KM, Kim CA, Messiaena LM. Multiple, diffuse schwannomas in a RASopathy phenotype patient with germline KRAS mutation [Carta]: a causal relationship? [Internet]. Clinical Genetics. 2012 ; 81( 6): 595-597.[citado 2024 ago. 11 ] Available from: https://doi.org/10.1111/j.1399-0004.2011.01764.x
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MURAT, C. B. et al. Mutation and genomic amplification of the PIK3CA proto-oncogene in pituitary adenomas. Brazilian Journal of Medical and Biological Research, v. 45, n. 9, p. 851-855, 2012Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x2012007500115. Acesso em: 11 ago. 2024.
APA
Murat, C. B., Braga, P. B. S., Fortes, M. A. H. Z., Bronstein, M. D., Corrêa-Giannella, M. L. C., & Giorgi, R. R. (2012). Mutation and genomic amplification of the PIK3CA proto-oncogene in pituitary adenomas. Brazilian Journal of Medical and Biological Research, 45( 9), 851-855. doi:10.1590/s0100-879x2012007500115
NLM
Murat CB, Braga PBS, Fortes MAHZ, Bronstein MD, Corrêa-Giannella MLC, Giorgi RR. Mutation and genomic amplification of the PIK3CA proto-oncogene in pituitary adenomas [Internet]. Brazilian Journal of Medical and Biological Research. 2012 ; 45( 9): 851-855.[citado 2024 ago. 11 ] Available from: https://doi.org/10.1590/s0100-879x2012007500115
Vancouver
Murat CB, Braga PBS, Fortes MAHZ, Bronstein MD, Corrêa-Giannella MLC, Giorgi RR. Mutation and genomic amplification of the PIK3CA proto-oncogene in pituitary adenomas [Internet]. Brazilian Journal of Medical and Biological Research. 2012 ; 45( 9): 851-855.[citado 2024 ago. 11 ] Available from: https://doi.org/10.1590/s0100-879x2012007500115
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TELES, M. G. et al. A novel homozygous splice acceptor site mutation of KISS1R in two siblings with normosmic isolated hypogonadotropic hypogonadism. European Journal of Endocrinology, v. 163, n. 1, p. 29-34, 2010Tradução . . Disponível em: https://doi.org/10.1530/EJE-10-0012. Acesso em: 11 ago. 2024.
APA
Teles, M. G., Trarbach, E. B., Noel, S. D., Guerra Junior, G., Beneduzzi, D., Bianco, S. D., et al. (2010). A novel homozygous splice acceptor site mutation of KISS1R in two siblings with normosmic isolated hypogonadotropic hypogonadism. European Journal of Endocrinology, 163( 1), 29-34. doi:10.1530/EJE-10-0012
NLM
Teles MG, Trarbach EB, Noel SD, Guerra Junior G, Beneduzzi D, Bianco SD, Jorge AAL, Mukherjee A, Baptista MT, Costa EM, Castro M de, Mendonça BB, Kaiser UB, Latronico AC. A novel homozygous splice acceptor site mutation of KISS1R in two siblings with normosmic isolated hypogonadotropic hypogonadism [Internet]. European Journal of Endocrinology. 2010 ; 163( 1): 29-34.[citado 2024 ago. 11 ] Available from: https://doi.org/10.1530/EJE-10-0012
Vancouver
Teles MG, Trarbach EB, Noel SD, Guerra Junior G, Beneduzzi D, Bianco SD, Jorge AAL, Mukherjee A, Baptista MT, Costa EM, Castro M de, Mendonça BB, Kaiser UB, Latronico AC. A novel homozygous splice acceptor site mutation of KISS1R in two siblings with normosmic isolated hypogonadotropic hypogonadism [Internet]. European Journal of Endocrinology. 2010 ; 163( 1): 29-34.[citado 2024 ago. 11 ] Available from: https://doi.org/10.1530/EJE-10-0012
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FUNKE, A. D. et al. The p.P56S mutation in the VAPB gene is not due to a single founder: first European case. [Letter to the editor]. Clinical Genetics, v. 77, n. 3, p. 302-303, 2010Tradução . . Acesso em: 11 ago. 2024.
APA
Funke, A. D., Esser, M., Krüttgen, A., Weis, J., Mitne Neto, M., Lazar, M., et al. (2010). The p.P56S mutation in the VAPB gene is not due to a single founder: first European case. [Letter to the editor]. Clinical Genetics, 77( 3), 302-303.
NLM
Funke AD, Esser M, Krüttgen A, Weis J, Mitne Neto M, Lazar M, Nishimura AL, Sperfela AD, Trillenberg P, Senderek J, Krasnianski M, Zatz M, Zierz S, Deschauer M. The p.P56S mutation in the VAPB gene is not due to a single founder: first European case. [Letter to the editor]. Clinical Genetics. 2010 ; 77( 3): 302-303.[citado 2024 ago. 11 ]
Vancouver
Funke AD, Esser M, Krüttgen A, Weis J, Mitne Neto M, Lazar M, Nishimura AL, Sperfela AD, Trillenberg P, Senderek J, Krasnianski M, Zatz M, Zierz S, Deschauer M. The p.P56S mutation in the VAPB gene is not due to a single founder: first European case. [Letter to the editor]. Clinical Genetics. 2010 ; 77( 3): 302-303.[citado 2024 ago. 11 ]
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PIRES, Patricia N. Pugliese et al. A novel STAT5B mutation causing GH insensitivity syndrome associated with hyperprolactinemia and immune dysfunction in two male siblings. European Journal of Endocrinology, v. 163, n. 2, p. 349-355, 2010Tradução . . Disponível em: https://doi.org/10.1530/EJE-10-0272. Acesso em: 11 ago. 2024.
APA
Pires, P. N. P., Tonelli, C. A., Dora, J. M., Silva, P. C. A., Czepielewski, M., Simoni, G., et al. (2010). A novel STAT5B mutation causing GH insensitivity syndrome associated with hyperprolactinemia and immune dysfunction in two male siblings. European Journal of Endocrinology, 163( 2), 349-355. doi:10.1530/EJE-10-0272
NLM
Pires PNP, Tonelli CA, Dora JM, Silva PCA, Czepielewski M, Simoni G, Arnhold IJP, Jorge AAL. A novel STAT5B mutation causing GH insensitivity syndrome associated with hyperprolactinemia and immune dysfunction in two male siblings [Internet]. European Journal of Endocrinology. 2010 ; 163( 2): 349-355.[citado 2024 ago. 11 ] Available from: https://doi.org/10.1530/EJE-10-0272
Vancouver
Pires PNP, Tonelli CA, Dora JM, Silva PCA, Czepielewski M, Simoni G, Arnhold IJP, Jorge AAL. A novel STAT5B mutation causing GH insensitivity syndrome associated with hyperprolactinemia and immune dysfunction in two male siblings [Internet]. European Journal of Endocrinology. 2010 ; 163( 2): 349-355.[citado 2024 ago. 11 ] Available from: https://doi.org/10.1530/EJE-10-0272
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BATISSOCO, Ana Carla et al. Prevalence of GJB2 (connexin-26) and GJB6 (connexin-30) mutations in a cohort of 300 brazilian hearing-impaired individuals: implications for diagnosis and genetic counseling. Ear and Hearing, v. 30, n. 1, p. 1-7, 2009Tradução . . Acesso em: 11 ago. 2024.
APA
Batissoco, A. C., Abreu-Silva, R. S., Braga, M. C. C., Lezirovitz, K., Della Rosa, V. A., Tabith Jr, A., et al. (2009). Prevalence of GJB2 (connexin-26) and GJB6 (connexin-30) mutations in a cohort of 300 brazilian hearing-impaired individuals: implications for diagnosis and genetic counseling. Ear and Hearing, 30( 1), 1-7.
NLM
Batissoco AC, Abreu-Silva RS, Braga MCC, Lezirovitz K, Della Rosa VA, Tabith Jr A, Otto PA, Mingroni Netto RC. Prevalence of GJB2 (connexin-26) and GJB6 (connexin-30) mutations in a cohort of 300 brazilian hearing-impaired individuals: implications for diagnosis and genetic counseling. Ear and Hearing. 2009 ; 30( 1): 1-7.[citado 2024 ago. 11 ]
Vancouver
Batissoco AC, Abreu-Silva RS, Braga MCC, Lezirovitz K, Della Rosa VA, Tabith Jr A, Otto PA, Mingroni Netto RC. Prevalence of GJB2 (connexin-26) and GJB6 (connexin-30) mutations in a cohort of 300 brazilian hearing-impaired individuals: implications for diagnosis and genetic counseling. Ear and Hearing. 2009 ; 30( 1): 1-7.[citado 2024 ago. 11 ]
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LEZIROVITZ, Karina et al. A novel association of a polymorphism in the first intron of adiponectin gene with type 2 diabetes, obesity and hypoadiponectinemia in Asian Indians. Human Genetics, v. 123, n. 6, p. 625-631, 2008Tradução . . Acesso em: 11 ago. 2024.
APA
Lezirovitz, K., Maestrelli, S. R. P., Cotrim, N. H., Otto, P. A., Pearson, P. L., & Mingroni Netto, R. C. (2008). A novel association of a polymorphism in the first intron of adiponectin gene with type 2 diabetes, obesity and hypoadiponectinemia in Asian Indians. Human Genetics, 123( 6), 625-631.
NLM
Lezirovitz K, Maestrelli SRP, Cotrim NH, Otto PA, Pearson PL, Mingroni Netto RC. A novel association of a polymorphism in the first intron of adiponectin gene with type 2 diabetes, obesity and hypoadiponectinemia in Asian Indians. Human Genetics. 2008 ; 123( 6): 625-631.[citado 2024 ago. 11 ]
Vancouver
Lezirovitz K, Maestrelli SRP, Cotrim NH, Otto PA, Pearson PL, Mingroni Netto RC. A novel association of a polymorphism in the first intron of adiponectin gene with type 2 diabetes, obesity and hypoadiponectinemia in Asian Indians. Human Genetics. 2008 ; 123( 6): 625-631.[citado 2024 ago. 11 ]
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MALAQUIAS, Alexsandra C. et al. Síndrome de Noonan: do Fenótipo à Terapêutica com Hormônio de Crescimento. Arquivos Brasileiros de Endocrinologia e Metabologia, v. 52, n. 5, p. 800-808, 2008Tradução . . Disponível em: http://www.scielo.br/pdf/abem/v52n4/a19v52n4.pdf. Acesso em: 11 ago. 2024.
APA
Malaquias, A. C., Ferreira, L. V., Souza, S. C., Arnhold, I. J. P., Mendonça, B. B., & Jorge, A. A. L. (2008). Síndrome de Noonan: do Fenótipo à Terapêutica com Hormônio de Crescimento. Arquivos Brasileiros de Endocrinologia e Metabologia, 52( 5), 800-808. Recuperado de http://www.scielo.br/pdf/abem/v52n4/a19v52n4.pdf
NLM
Malaquias AC, Ferreira LV, Souza SC, Arnhold IJP, Mendonça BB, Jorge AAL. Síndrome de Noonan: do Fenótipo à Terapêutica com Hormônio de Crescimento [Internet]. Arquivos Brasileiros de Endocrinologia e Metabologia. 2008 ; 52( 5): 800-808.[citado 2024 ago. 11 ] Available from: http://www.scielo.br/pdf/abem/v52n4/a19v52n4.pdf
Vancouver
Malaquias AC, Ferreira LV, Souza SC, Arnhold IJP, Mendonça BB, Jorge AAL. Síndrome de Noonan: do Fenótipo à Terapêutica com Hormônio de Crescimento [Internet]. Arquivos Brasileiros de Endocrinologia e Metabologia. 2008 ; 52( 5): 800-808.[citado 2024 ago. 11 ] Available from: http://www.scielo.br/pdf/abem/v52n4/a19v52n4.pdf
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RUBIO, Ileana G. S. et al. A molecular analysis and long-term follow-up of two siblings with severe congenital hypothyroidism carrying the IVS30+1G>T intronic thyroglobulin mutation. Arquivos Brasileiros de Endocrinologia e Metabologia, v. 52, n. 8, p. 1337-1344, 2008Tradução . . Disponível em: https://doi.org/10.1590/s0004-27302008000800022. Acesso em: 11 ago. 2024.
APA
Rubio, I. G. S., Galrao, A. L., Pardo, V., Knobel, M., Possato, R. F., Camargo, R. R. Y., et al. (2008). A molecular analysis and long-term follow-up of two siblings with severe congenital hypothyroidism carrying the IVS30+1G>T intronic thyroglobulin mutation. Arquivos Brasileiros de Endocrinologia e Metabologia, 52( 8), 1337-1344. doi:10.1590/s0004-27302008000800022
NLM
Rubio IGS, Galrao AL, Pardo V, Knobel M, Possato RF, Camargo RRY, Ferreira MA, Kanamura CT, Gomes SA, Medeiros-Neto G. A molecular analysis and long-term follow-up of two siblings with severe congenital hypothyroidism carrying the IVS30+1G>T intronic thyroglobulin mutation [Internet]. Arquivos Brasileiros de Endocrinologia e Metabologia. 2008 ; 52( 8): 1337-1344.[citado 2024 ago. 11 ] Available from: https://doi.org/10.1590/s0004-27302008000800022
Vancouver
Rubio IGS, Galrao AL, Pardo V, Knobel M, Possato RF, Camargo RRY, Ferreira MA, Kanamura CT, Gomes SA, Medeiros-Neto G. A molecular analysis and long-term follow-up of two siblings with severe congenital hypothyroidism carrying the IVS30+1G>T intronic thyroglobulin mutation [Internet]. Arquivos Brasileiros de Endocrinologia e Metabologia. 2008 ; 52( 8): 1337-1344.[citado 2024 ago. 11 ] Available from: https://doi.org/10.1590/s0004-27302008000800022
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KOSSUGUE, Patricia Mayumi et al. Central core disease due to recessive mutations in RYR1 gene: is it more common than described?. Muscle & Nerve, v. 35, n. 5, p. 670-674, 2007Tradução . . Disponível em: https://doi.org/10.1002/mus.20715. Acesso em: 11 ago. 2024.
APA
Kossugue, P. M., Paim, J. F., Navarro, M. M., Silva, H. C. A. da, Pavanello, R. de C. M., Gurgel-Giannetti, J., et al. (2007). Central core disease due to recessive mutations in RYR1 gene: is it more common than described? Muscle & Nerve, 35( 5), 670-674. doi:10.1002/mus.20715
NLM
Kossugue PM, Paim JF, Navarro MM, Silva HCA da, Pavanello R de CM, Gurgel-Giannetti J, Zatz M, Vainzof M. Central core disease due to recessive mutations in RYR1 gene: is it more common than described? [Internet]. Muscle & Nerve. 2007 ; 35( 5): 670-674.[citado 2024 ago. 11 ] Available from: https://doi.org/10.1002/mus.20715
Vancouver
Kossugue PM, Paim JF, Navarro MM, Silva HCA da, Pavanello R de CM, Gurgel-Giannetti J, Zatz M, Vainzof M. Central core disease due to recessive mutations in RYR1 gene: is it more common than described? [Internet]. Muscle & Nerve. 2007 ; 35( 5): 670-674.[citado 2024 ago. 11 ] Available from: https://doi.org/10.1002/mus.20715
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GOUVEIA, Telma Luciana Furtado et al. A new evidence for the maintenance of the sarcoglycan complex in muscle sarcolemma in spite of the primary absence of 'delta'-SG protein. Journal of Molecular Medicine, v. 85, n. 4, p. 415-420, 2007Tradução . . Disponível em: https://doi.org/10.1007/s00109-007-0163-8. Acesso em: 11 ago. 2024.
APA
Gouveia, T. L. F., Kossugue, P. M., Paim, J. F., Zatz, M., Anderson, L. V. B., Nigro, V., & Vainzof, M. (2007). A new evidence for the maintenance of the sarcoglycan complex in muscle sarcolemma in spite of the primary absence of 'delta'-SG protein. Journal of Molecular Medicine, 85( 4), 415-420. doi:10.1007/s00109-007-0163-8
NLM
Gouveia TLF, Kossugue PM, Paim JF, Zatz M, Anderson LVB, Nigro V, Vainzof M. A new evidence for the maintenance of the sarcoglycan complex in muscle sarcolemma in spite of the primary absence of 'delta'-SG protein [Internet]. Journal of Molecular Medicine. 2007 ; 85( 4): 415-420.[citado 2024 ago. 11 ] Available from: https://doi.org/10.1007/s00109-007-0163-8
Vancouver
Gouveia TLF, Kossugue PM, Paim JF, Zatz M, Anderson LVB, Nigro V, Vainzof M. A new evidence for the maintenance of the sarcoglycan complex in muscle sarcolemma in spite of the primary absence of 'delta'-SG protein [Internet]. Journal of Molecular Medicine. 2007 ; 85( 4): 415-420.[citado 2024 ago. 11 ] Available from: https://doi.org/10.1007/s00109-007-0163-8
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SCHMIDT, Wolfgang M. et al. Mutation in the Scyl1 gene encoding amino-terminal kinase-like protein causes a recessive form of spinocerebellar neurodegeneration. EMBO reports, v. 8, n. 7, p. 691-697, 2007Tradução . . Disponível em: https://doi.org/10.1038/sj.embor.7401001. Acesso em: 11 ago. 2024.
APA
Schmidt, W. M., Kraus, C., Höger, H., Oberndorfer, F., Branka, M., Bingemann, S., et al. (2007). Mutation in the Scyl1 gene encoding amino-terminal kinase-like protein causes a recessive form of spinocerebellar neurodegeneration. EMBO reports, 8( 7), 691-697. doi:10.1038/sj.embor.7401001
NLM
Schmidt WM, Kraus C, Höger H, Oberndorfer F, Branka M, Bingemann S, Lassmann H, Müller M, Macedo-Souza LI, Vainzof M, Zatz M, Reis A, Bittner RE. Mutation in the Scyl1 gene encoding amino-terminal kinase-like protein causes a recessive form of spinocerebellar neurodegeneration [Internet]. EMBO reports. 2007 ; 8( 7): 691-697.[citado 2024 ago. 11 ] Available from: https://doi.org/10.1038/sj.embor.7401001
Vancouver
Schmidt WM, Kraus C, Höger H, Oberndorfer F, Branka M, Bingemann S, Lassmann H, Müller M, Macedo-Souza LI, Vainzof M, Zatz M, Reis A, Bittner RE. Mutation in the Scyl1 gene encoding amino-terminal kinase-like protein causes a recessive form of spinocerebellar neurodegeneration [Internet]. EMBO reports. 2007 ; 8( 7): 691-697.[citado 2024 ago. 11 ] Available from: https://doi.org/10.1038/sj.embor.7401001
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
COSTA, Marcelo Fernandes da et al. Red-green color vision impairment in Duchenne Muscular Dystrophy. American Journal of Human Genetics, v. 80, n. 6, p. 1064-1075, 2007Tradução . . Acesso em: 11 ago. 2024.
APA
Costa, M. F. da, Oliveira, A. G. F., Feitosa-Santana, C., Zatz, M., & Ventura, D. S. F. (2007). Red-green color vision impairment in Duchenne Muscular Dystrophy. American Journal of Human Genetics, 80( 6), 1064-1075.
NLM
Costa MF da, Oliveira AGF, Feitosa-Santana C, Zatz M, Ventura DSF. Red-green color vision impairment in Duchenne Muscular Dystrophy. American Journal of Human Genetics. 2007 ; 80( 6): 1064-1075.[citado 2024 ago. 11 ]
Vancouver
Costa MF da, Oliveira AGF, Feitosa-Santana C, Zatz M, Ventura DSF. Red-green color vision impairment in Duchenne Muscular Dystrophy. American Journal of Human Genetics. 2007 ; 80( 6): 1064-1075.[citado 2024 ago. 11 ]
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ABREU-SILVA, Ronaldo Serafim et al. Correspondence regarding Ballana et al., "Mitochondrial 12S rRNA gene mutations affect RNA secondary structure and lead to variable penetrance in hearing impairment". Biochemical and Biophysical Research Communications, v. 343, n. 3, p. 675-676, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.bbrc.2006.03.049. Acesso em: 11 ago. 2024.
APA
Abreu-Silva, R. S., Batissoco, A. C., Lezirovitz, K., Romanos, J., Rincon, D., Auricchio, M. T. B. de M., et al. (2006). Correspondence regarding Ballana et al., "Mitochondrial 12S rRNA gene mutations affect RNA secondary structure and lead to variable penetrance in hearing impairment". Biochemical and Biophysical Research Communications, 343( 3), 675-676. doi:10.1016/j.bbrc.2006.03.049
NLM
Abreu-Silva RS, Batissoco AC, Lezirovitz K, Romanos J, Rincon D, Auricchio MTB de M, Otto PA, Mingroni Netto RC. Correspondence regarding Ballana et al., "Mitochondrial 12S rRNA gene mutations affect RNA secondary structure and lead to variable penetrance in hearing impairment" [Internet]. Biochemical and Biophysical Research Communications. 2006 ; 343( 3): 675-676.[citado 2024 ago. 11 ] Available from: https://doi.org/10.1016/j.bbrc.2006.03.049
Vancouver
Abreu-Silva RS, Batissoco AC, Lezirovitz K, Romanos J, Rincon D, Auricchio MTB de M, Otto PA, Mingroni Netto RC. Correspondence regarding Ballana et al., "Mitochondrial 12S rRNA gene mutations affect RNA secondary structure and lead to variable penetrance in hearing impairment" [Internet]. Biochemical and Biophysical Research Communications. 2006 ; 343( 3): 675-676.[citado 2024 ago. 11 ] Available from: https://doi.org/10.1016/j.bbrc.2006.03.049