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Artigo de periodico
The search of a genetic basis for noise-induced hearing loss (NIHL) (2011)
Abreu-Silva, Ronaldo Serafim; Rincon, Daniel; Horimoto, Andréa Roseli Vançan Russo; Sguillar, Ary Papa; Ricardo, Luiz Artur Costa; Kimura, Lilian; Batissoco, Ana Carla; Auricchio, Maria Teresa Ballester de Melo; Otto, Paulo A ; Mingroni Netto, Regina Celia
Source: Annals of Human Biology. Unidade: IB
Subjects: SURDEZ, MUTAÇÃO GENÉTICA
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ABNT
ABREU-SILVA, Ronaldo Serafim et al. The search of a genetic basis for noise-induced hearing loss (NIHL). Annals of Human Biology, v. 38, n. 2, p. 210-218, 2011Tradução . . Disponível em: https://doi.org/10.3109/03014460.2010.513774. Acesso em: 26 set. 2024.
APA
Abreu-Silva, R. S., Rincon, D., Horimoto, A. R. V. R., Sguillar, A. P., Ricardo, L. A. C., Kimura, L., et al. (2011). The search of a genetic basis for noise-induced hearing loss (NIHL). Annals of Human Biology, 38( 2), 210-218. doi:10.3109/03014460.2010.513774
NLM
Abreu-Silva RS, Rincon D, Horimoto ARVR, Sguillar AP, Ricardo LAC, Kimura L, Batissoco AC, Auricchio MTB de M, Otto PA, Mingroni Netto RC. The search of a genetic basis for noise-induced hearing loss (NIHL) [Internet]. Annals of Human Biology. 2011 ; 38( 2): 210-218.[citado 2024 set. 26 ] Available from: https://doi.org/10.3109/03014460.2010.513774
Vancouver
Abreu-Silva RS, Rincon D, Horimoto ARVR, Sguillar AP, Ricardo LAC, Kimura L, Batissoco AC, Auricchio MTB de M, Otto PA, Mingroni Netto RC. The search of a genetic basis for noise-induced hearing loss (NIHL) [Internet]. Annals of Human Biology. 2011 ; 38( 2): 210-218.[citado 2024 set. 26 ] Available from: https://doi.org/10.3109/03014460.2010.513774
Artigo de periodico
Chromosome imbalances in syndromic hearing loss (2009)
Catelani, A.L.P.M.; Krepischi, Ana Cristina Victorino ; Kim, C. A.; Kok, Fernando; Otto, Paulo A ; Auricchio, Maria Teresa Ballester de Melo; Mazzeu, Juliana Forte; Uehara, D. T.; Costa, S. S.; Knijnenburg, Jeroen; Tabith Junior, Alfredo; Vianna-Morgante, Angela M ; Mingroni Netto, Regina Celia ; Rosenberg, Carla
Source: Clinical Genetics. Unidade: IB
Subjects: CROMOSSOMOS, MUTAÇÃO GENÉTICA, SURDEZ
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ABNT
CATELANI, A.L.P.M. et al. Chromosome imbalances in syndromic hearing loss. Clinical Genetics, v. 76, n. 5, p. 458-464, 2009Tradução . . Disponível em: https://doi.org/10.1111/j.1399-0004.2009.01276.x. Acesso em: 26 set. 2024.
APA
Catelani, A. L. P. M., Krepischi, A. C. V., Kim, C. A., Kok, F., Otto, P. A., Auricchio, M. T. B. de M., et al. (2009). Chromosome imbalances in syndromic hearing loss. Clinical Genetics, 76( 5), 458-464. doi:10.1111/j.1399-0004.2009.01276.x
NLM
Catelani ALPM, Krepischi ACV, Kim CA, Kok F, Otto PA, Auricchio MTB de M, Mazzeu JF, Uehara DT, Costa SS, Knijnenburg J, Tabith Junior A, Vianna-Morgante AM, Mingroni Netto RC, Rosenberg C. Chromosome imbalances in syndromic hearing loss [Internet]. Clinical Genetics. 2009 ; 76( 5): 458-464.[citado 2024 set. 26 ] Available from: https://doi.org/10.1111/j.1399-0004.2009.01276.x
Vancouver
Catelani ALPM, Krepischi ACV, Kim CA, Kok F, Otto PA, Auricchio MTB de M, Mazzeu JF, Uehara DT, Costa SS, Knijnenburg J, Tabith Junior A, Vianna-Morgante AM, Mingroni Netto RC, Rosenberg C. Chromosome imbalances in syndromic hearing loss [Internet]. Clinical Genetics. 2009 ; 76( 5): 458-464.[citado 2024 set. 26 ] Available from: https://doi.org/10.1111/j.1399-0004.2009.01276.x
Artigo de periodico
Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents (2006)
Rosenberg, Carla ; Knijnenburg, Jeroen; Bakker, E; Vianna-Morgante, Angela M ; Sloos, W.; Otto, Paulo A ; Kriek, M.; Hansson, K.; Krepischi, Ana Cristina Victorino ; Fiegler, H.; Carter, N. P.; Bijlsma, E. K.; Van Haeringen, A.; Szuhai, K.; Tanke, H. J.
Source: Journal of Medical Genetics. Unidade: IB
Subjects: RETARDO MENTAL, DOENÇAS GENÉTICAS
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ABNT
ROSENBERG, Carla et al. Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents. Journal of Medical Genetics, v. 43, p. 180-186, 2006Tradução . . Disponível em: https://doi.org/10.1136/jmg.2005.032268. Acesso em: 26 set. 2024.
APA
Rosenberg, C., Knijnenburg, J., Bakker, E., Vianna-Morgante, A. M., Sloos, W., Otto, P. A., et al. (2006). Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents. Journal of Medical Genetics, 43, 180-186. doi:10.1136/jmg.2005.032268
NLM
Rosenberg C, Knijnenburg J, Bakker E, Vianna-Morgante AM, Sloos W, Otto PA, Kriek M, Hansson K, Krepischi ACV, Fiegler H, Carter NP, Bijlsma EK, Van Haeringen A, Szuhai K, Tanke HJ. Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents [Internet]. Journal of Medical Genetics. 2006 ; 43 180-186.[citado 2024 set. 26 ] Available from: https://doi.org/10.1136/jmg.2005.032268
Vancouver
Rosenberg C, Knijnenburg J, Bakker E, Vianna-Morgante AM, Sloos W, Otto PA, Kriek M, Hansson K, Krepischi ACV, Fiegler H, Carter NP, Bijlsma EK, Van Haeringen A, Szuhai K, Tanke HJ. Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents [Internet]. Journal of Medical Genetics. 2006 ; 43 180-186.[citado 2024 set. 26 ] Available from: https://doi.org/10.1136/jmg.2005.032268
Artigo de periodico
Phenotypic variability in Angelman syndrome: comparison among different deletion classes and between deletion and UPD subjects (2004)
Varela, Monica Castro; Kok, Fernando; Otto, Paulo A ; Koiffmann, Celia Priszkulnik
Source: European Journal of Human Genetics. Unidade: IB
Subjects: SÍNDROME DE ANGELMAN, DELEÇÃO DE GENES
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ABNT
VARELA, Monica Castro et al. Phenotypic variability in Angelman syndrome: comparison among different deletion classes and between deletion and UPD subjects. European Journal of Human Genetics, p. 987-992, 2004Tradução . . Disponível em: https://doi.org/10.1038/sj.ejhg.5201264. Acesso em: 26 set. 2024.
APA
Varela, M. C., Kok, F., Otto, P. A., & Koiffmann, C. P. (2004). Phenotypic variability in Angelman syndrome: comparison among different deletion classes and between deletion and UPD subjects. European Journal of Human Genetics, 987-992. doi:10.1038/sj.ejhg.5201264
NLM
Varela MC, Kok F, Otto PA, Koiffmann CP. Phenotypic variability in Angelman syndrome: comparison among different deletion classes and between deletion and UPD subjects [Internet]. European Journal of Human Genetics. 2004 ; 987-992.[citado 2024 set. 26 ] Available from: https://doi.org/10.1038/sj.ejhg.5201264
Vancouver
Varela MC, Kok F, Otto PA, Koiffmann CP. Phenotypic variability in Angelman syndrome: comparison among different deletion classes and between deletion and UPD subjects [Internet]. European Journal of Human Genetics. 2004 ; 987-992.[citado 2024 set. 26 ] Available from: https://doi.org/10.1038/sj.ejhg.5201264
Artigo de periodico
Polymorphic Alu insertions in six brazilian african-derived populations (2004)
Cotrim, Nelson Henderson; Auricchio, Maria Teresa B. M.; Vicente, João Pedro; Otto, Paulo A ; Mingroni Netto, Regina Celia
Source: American Journal of Human Biology. Unidade: IB
Subjects: GENÉTICA DE POPULAÇÕES, QUILOMBOS
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ABNT
COTRIM, Nelson Henderson et al. Polymorphic Alu insertions in six brazilian african-derived populations. American Journal of Human Biology, v. 16, n. 3, p. 264-277, 2004Tradução . . Disponível em: https://doi.org/10.1002/ajhb.20024. Acesso em: 26 set. 2024.
APA
Cotrim, N. H., Auricchio, M. T. B. M., Vicente, J. P., Otto, P. A., & Mingroni Netto, R. C. (2004). Polymorphic Alu insertions in six brazilian african-derived populations. American Journal of Human Biology, 16( 3), 264-277. doi:10.1002/ajhb.20024
NLM
Cotrim NH, Auricchio MTBM, Vicente JP, Otto PA, Mingroni Netto RC. Polymorphic Alu insertions in six brazilian african-derived populations [Internet]. American Journal of Human Biology. 2004 ; 16( 3): 264-277.[citado 2024 set. 26 ] Available from: https://doi.org/10.1002/ajhb.20024
Vancouver
Cotrim NH, Auricchio MTBM, Vicente JP, Otto PA, Mingroni Netto RC. Polymorphic Alu insertions in six brazilian african-derived populations [Internet]. American Journal of Human Biology. 2004 ; 16( 3): 264-277.[citado 2024 set. 26 ] Available from: https://doi.org/10.1002/ajhb.20024
Artigo de periodico
Replication timing of homologous 'alfa'-satelite DNA in Roberts syndrome (2000)
Barbosa, Ana Carolina Coutinho; Otto, Paulo A ; Vianna-Morgante, Angela M
Source: Chromosome Research. Unidade: IB
Assunto: GENÉTICA MÉDICA
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ABNT
BARBOSA, Ana Carolina Coutinho e OTTO, Paulo A e VIANNA-MORGANTE, Angela M. Replication timing of homologous 'alfa'-satelite DNA in Roberts syndrome. Chromosome Research, v. 8, p. 645-650, 2000Tradução . . Acesso em: 26 set. 2024.
APA
Barbosa, A. C. C., Otto, P. A., & Vianna-Morgante, A. M. (2000). Replication timing of homologous 'alfa'-satelite DNA in Roberts syndrome. Chromosome Research, 8, 645-650.
NLM
Barbosa ACC, Otto PA, Vianna-Morgante AM. Replication timing of homologous 'alfa'-satelite DNA in Roberts syndrome. Chromosome Research. 2000 ; 8 645-650.[citado 2024 set. 26 ]
Vancouver
Barbosa ACC, Otto PA, Vianna-Morgante AM. Replication timing of homologous 'alfa'-satelite DNA in Roberts syndrome. Chromosome Research. 2000 ; 8 645-650.[citado 2024 set. 26 ]
Artigo de periodico
Estimation of penetrance from twin data (2000)
Praxedes, Leide de Almeida; Otto, Paulo A
Source: Twin Research. Unidade: IB
Assunto: GENÉTICA (ESTATÍSTICAS E DADOS NUMÉRICOS)
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ABNT
PRAXEDES, Leide de Almeida e OTTO, Paulo A. Estimation of penetrance from twin data. Twin Research, v. 3, p. 294-298, 2000Tradução . . Disponível em: https://doi.org/10.1375/twin.3.4.294. Acesso em: 26 set. 2024.
APA
Praxedes, L. de A., & Otto, P. A. (2000). Estimation of penetrance from twin data. Twin Research, 3, 294-298. doi:10.1375/twin.3.4.294
NLM
Praxedes L de A, Otto PA. Estimation of penetrance from twin data [Internet]. Twin Research. 2000 ; 3 294-298.[citado 2024 set. 26 ] Available from: https://doi.org/10.1375/twin.3.4.294
Vancouver
Praxedes L de A, Otto PA. Estimation of penetrance from twin data [Internet]. Twin Research. 2000 ; 3 294-298.[citado 2024 set. 26 ] Available from: https://doi.org/10.1375/twin.3.4.294
Artigo de periodico
The association of the short variant of the 5-HTTPLR polymorphism and the apoE 'épsilon'4 allele does not increase the risk for late onset Alzheimer's disease (1999)
Oliveira, J. R. M.; Shimokomaki, C M; Brito-Marques, P R; Gallindo, R M; Okuma, M; Maia, L G S; Otto, Paulo A ; Passos-Bueno, Maria Rita ; Zatz, Mayana
Source: Molecular Psychiatry. Unidade: IB
Assunto: GENÉTICA MÉDICA
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ABNT
OLIVEIRA, J. R. M. et al. The association of the short variant of the 5-HTTPLR polymorphism and the apoE 'épsilon'4 allele does not increase the risk for late onset Alzheimer's disease. Molecular Psychiatry, v. 4, p. 19-20, 1999Tradução . . Disponível em: https://doi.org/10.1038/sj.mp.4000493. Acesso em: 26 set. 2024.
APA
Oliveira, J. R. M., Shimokomaki, C. M., Brito-Marques, P. R., Gallindo, R. M., Okuma, M., Maia, L. G. S., et al. (1999). The association of the short variant of the 5-HTTPLR polymorphism and the apoE 'épsilon'4 allele does not increase the risk for late onset Alzheimer's disease. Molecular Psychiatry, 4, 19-20. doi:10.1038/sj.mp.4000493
NLM
Oliveira JRM, Shimokomaki CM, Brito-Marques PR, Gallindo RM, Okuma M, Maia LGS, Otto PA, Passos-Bueno MR, Zatz M. The association of the short variant of the 5-HTTPLR polymorphism and the apoE 'épsilon'4 allele does not increase the risk for late onset Alzheimer's disease [Internet]. Molecular Psychiatry. 1999 ; 4 19-20.[citado 2024 set. 26 ] Available from: https://doi.org/10.1038/sj.mp.4000493
Vancouver
Oliveira JRM, Shimokomaki CM, Brito-Marques PR, Gallindo RM, Okuma M, Maia LGS, Otto PA, Passos-Bueno MR, Zatz M. The association of the short variant of the 5-HTTPLR polymorphism and the apoE 'épsilon'4 allele does not increase the risk for late onset Alzheimer's disease [Internet]. Molecular Psychiatry. 1999 ; 4 19-20.[citado 2024 set. 26 ] Available from: https://doi.org/10.1038/sj.mp.4000493
Artigo de periodico-carta/editorial
Risk of 45,X karyotype in offspring of turner's syndrome patients. [Letters to the editor] (1977)
Otto, Paulo A ; Kasahara, Sanae; Nunesmaia, Henrique Gil da Silva; Frota-Pessoa, Oswaldo
Source: Lancet. Unidade: IB
Assunto: CARIOTIPAGEM
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ABNT
OTTO, Paulo A et al. Risk of 45,X karyotype in offspring of turner's syndrome patients. [Letters to the editor]. Lancet. London: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 26 set. 2024. , 1977
APA
Otto, P. A., Kasahara, S., Nunesmaia, H. G. da S., & Frota-Pessoa, O. (1977). Risk of 45,X karyotype in offspring of turner's syndrome patients. [Letters to the editor]. Lancet. London: Instituto de Biociências, Universidade de São Paulo.
NLM
Otto PA, Kasahara S, Nunesmaia HG da S, Frota-Pessoa O. Risk of 45,X karyotype in offspring of turner's syndrome patients. [Letters to the editor]. Lancet. 1977 ; 2 257.[citado 2024 set. 26 ]
Vancouver
Otto PA, Kasahara S, Nunesmaia HG da S, Frota-Pessoa O. Risk of 45,X karyotype in offspring of turner's syndrome patients. [Letters to the editor]. Lancet. 1977 ; 2 257.[citado 2024 set. 26 ]
Artigo de periodico
X-linked recessive type of pure spastic paraplegia in a large pedigree: absence of detectable linkage with Xg (1976)
Zatz, Mayana ; Penha-Serrano, Creuza; Otto, Paulo A
Source: Journal of Medical Genetics. Unidade: IB
Assunto: DOENÇAS HEREDITÁRIAS
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ABNT
ZATZ, Mayana e PENHA-SERRANO, Creuza e OTTO, Paulo A. X-linked recessive type of pure spastic paraplegia in a large pedigree: absence of detectable linkage with Xg. Journal of Medical Genetics, v. 13, n. 3, p. 217-222, 1976Tradução . . Disponível em: https://doi.org/10.1136/jmg.13.3.217. Acesso em: 26 set. 2024.
APA
Zatz, M., Penha-Serrano, C., & Otto, P. A. (1976). X-linked recessive type of pure spastic paraplegia in a large pedigree: absence of detectable linkage with Xg. Journal of Medical Genetics, 13( 3), 217-222. doi:10.1136/jmg.13.3.217
NLM
Zatz M, Penha-Serrano C, Otto PA. X-linked recessive type of pure spastic paraplegia in a large pedigree: absence of detectable linkage with Xg [Internet]. Journal of Medical Genetics. 1976 ; 13( 3): 217-222.[citado 2024 set. 26 ] Available from: https://doi.org/10.1136/jmg.13.3.217
Vancouver
Zatz M, Penha-Serrano C, Otto PA. X-linked recessive type of pure spastic paraplegia in a large pedigree: absence of detectable linkage with Xg [Internet]. Journal of Medical Genetics. 1976 ; 13( 3): 217-222.[citado 2024 set. 26 ] Available from: https://doi.org/10.1136/jmg.13.3.217

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