ReP USP - Resultado da busca

Artigo de periodico
Analysis of the genetic variability in a sample of the remaining group of Spix's Macaw (Cyanopsitta spixii, Psittaciformes: aves) by DNA fingerprinting (2001)
Caparroz, Renato ; Miyaki, Cristina Yumi ; Bampi, Maria I.; Wajntal, Anita
Source: Biological Conservation. Unidade: IB
Subjects: AVES, GENÉTICA ANIMAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CAPARROZ, Renato et al. Analysis of the genetic variability in a sample of the remaining group of Spix's Macaw (Cyanopsitta spixii, Psittaciformes: aves) by DNA fingerprinting. Biological Conservation, v. 99, p. 307-311, 2001Tradução . . Disponível em: https://doi.org/10.1016/s0006-3207(00)00196-8. Acesso em: 01 nov. 2024.
APA
Caparroz, R., Miyaki, C. Y., Bampi, M. I., & Wajntal, A. (2001). Analysis of the genetic variability in a sample of the remaining group of Spix's Macaw (Cyanopsitta spixii, Psittaciformes: aves) by DNA fingerprinting. Biological Conservation, 99, 307-311. doi:10.1016/s0006-3207(00)00196-8
NLM
Caparroz R, Miyaki CY, Bampi MI, Wajntal A. Analysis of the genetic variability in a sample of the remaining group of Spix's Macaw (Cyanopsitta spixii, Psittaciformes: aves) by DNA fingerprinting [Internet]. Biological Conservation. 2001 ; 99 307-311.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/s0006-3207(00)00196-8
Vancouver
Caparroz R, Miyaki CY, Bampi MI, Wajntal A. Analysis of the genetic variability in a sample of the remaining group of Spix's Macaw (Cyanopsitta spixii, Psittaciformes: aves) by DNA fingerprinting [Internet]. Biological Conservation. 2001 ; 99 307-311.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/s0006-3207(00)00196-8
Artigo de periodico
Mitochondrial DNA characterization of five species of Plebeia (Apidae: Meliponini): RFLP and restriction maps (2001)
Francisco, Flávio de Oliveira; Silvestre, Daniela; Arias, Maria Cristina
Source: Apidologie. Unidade: IB
Subjects: ABELHAS, DNA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FRANCISCO, Flávio de Oliveira e SILVESTRE, Daniela e ARIAS, Maria Cristina. Mitochondrial DNA characterization of five species of Plebeia (Apidae: Meliponini): RFLP and restriction maps. Apidologie, v. 32, p. 323-332, 2001Tradução . . Disponível em: https://doi.org/10.1051/apido:2001132. Acesso em: 01 nov. 2024.
APA
Francisco, F. de O., Silvestre, D., & Arias, M. C. (2001). Mitochondrial DNA characterization of five species of Plebeia (Apidae: Meliponini): RFLP and restriction maps. Apidologie, 32, 323-332. doi:10.1051/apido:2001132
NLM
Francisco F de O, Silvestre D, Arias MC. Mitochondrial DNA characterization of five species of Plebeia (Apidae: Meliponini): RFLP and restriction maps [Internet]. Apidologie. 2001 ; 32 323-332.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1051/apido:2001132
Vancouver
Francisco F de O, Silvestre D, Arias MC. Mitochondrial DNA characterization of five species of Plebeia (Apidae: Meliponini): RFLP and restriction maps [Internet]. Apidologie. 2001 ; 32 323-332.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1051/apido:2001132
Artigo de periodico
Mutations in the Caveolin-3 gene: when are they pathogenic? (2001)
Paula, Flavia de; Vainzof, Mariz ; Bernardino, Andréa L. F.; McNally, Elizabeth; Kunkel, Louis M; Zatz, Mayana
Source: American Journal of Medical Genetics. Unidade: IB
Subjects: GENÉTICA MÉDICA, DISTROFIA MUSCULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PAULA, Flavia de et al. Mutations in the Caveolin-3 gene: when are they pathogenic?. American Journal of Medical Genetics, v. 99, p. 303-307, 2001Tradução . . Disponível em: https://doi.org/10.1002/1096-8628(2001)9999:9999%3C::aid-ajmg1168%3E3.0.co;2-o. Acesso em: 01 nov. 2024.
APA
Paula, F. de, Vainzof, M., Bernardino, A. L. F., McNally, E., Kunkel, L. M., & Zatz, M. (2001). Mutations in the Caveolin-3 gene: when are they pathogenic? American Journal of Medical Genetics, 99, 303-307. doi:10.1002/1096-8628(2001)9999:9999%3C::aid-ajmg1168%3E3.0.co;2-o
NLM
Paula F de, Vainzof M, Bernardino ALF, McNally E, Kunkel LM, Zatz M. Mutations in the Caveolin-3 gene: when are they pathogenic? [Internet]. American Journal of Medical Genetics. 2001 ; 99 303-307.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1002/1096-8628(2001)9999:9999%3C::aid-ajmg1168%3E3.0.co;2-o
Vancouver
Paula F de, Vainzof M, Bernardino ALF, McNally E, Kunkel LM, Zatz M. Mutations in the Caveolin-3 gene: when are they pathogenic? [Internet]. American Journal of Medical Genetics. 2001 ; 99 303-307.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1002/1096-8628(2001)9999:9999%3C::aid-ajmg1168%3E3.0.co;2-o
Artigo de periodico
High mutation detection rate in TCOF1 among treacher Collins Syndrome patients reveals clustering of mutation and 16 novel pathogenic changes (2000)
Splendore, Alessandra; Silva, Elias Oliveira da; Alonso, Luís G.; Richieri-Costa, Antonio; Alonso, Nivaldo; Rosa, Alberto; Carakushansky, Gerson; Cavalcanti, Denise Pontes; Brunoni, Décio; Passos-Bueno, Maria Rita
Source: Human Mutation. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SPLENDORE, Alessandra et al. High mutation detection rate in TCOF1 among treacher Collins Syndrome patients reveals clustering of mutation and 16 novel pathogenic changes. Human Mutation, v. 16, p. 315-322, 2000Tradução . . Disponível em: https://doi.org/10.1002/1098-1004(200010)16:4%3C315::aid-humu4%3E3.0.co;2-h. Acesso em: 01 nov. 2024.
APA
Splendore, A., Silva, E. O. da, Alonso, L. G., Richieri-Costa, A., Alonso, N., Rosa, A., et al. (2000). High mutation detection rate in TCOF1 among treacher Collins Syndrome patients reveals clustering of mutation and 16 novel pathogenic changes. Human Mutation, 16, 315-322. doi:10.1002/1098-1004(200010)16:4%3C315::aid-humu4%3E3.0.co;2-h
NLM
Splendore A, Silva EO da, Alonso LG, Richieri-Costa A, Alonso N, Rosa A, Carakushansky G, Cavalcanti DP, Brunoni D, Passos-Bueno MR. High mutation detection rate in TCOF1 among treacher Collins Syndrome patients reveals clustering of mutation and 16 novel pathogenic changes [Internet]. Human Mutation. 2000 ; 16 315-322.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1002/1098-1004(200010)16:4%3C315::aid-humu4%3E3.0.co;2-h
Vancouver
Splendore A, Silva EO da, Alonso LG, Richieri-Costa A, Alonso N, Rosa A, Carakushansky G, Cavalcanti DP, Brunoni D, Passos-Bueno MR. High mutation detection rate in TCOF1 among treacher Collins Syndrome patients reveals clustering of mutation and 16 novel pathogenic changes [Internet]. Human Mutation. 2000 ; 16 315-322.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1002/1098-1004(200010)16:4%3C315::aid-humu4%3E3.0.co;2-h
Artigo de periodico
Catalases and thioredoxin peroxidase protect Saccharomyces cerevisiae against 'Ca POT.2+'-induced mitochondrial membrane permeabilization and cell death (2000)
Kowaltowski, Alicia Juliana ; Vercesi, Anibal E; Rhee, Sue Goo; Netto, Luis Eduardo Soares
Source: FEBS Letters. Unidade: IB
Assunto: BIOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KOWALTOWSKI, Alicia Juliana et al. Catalases and thioredoxin peroxidase protect Saccharomyces cerevisiae against 'Ca POT.2+'-induced mitochondrial membrane permeabilization and cell death. FEBS Letters, v. 473, p. 177-182, 2000Tradução . . Disponível em: https://doi.org/10.1016/s0014-5793(00)01526-x. Acesso em: 01 nov. 2024.
APA
Kowaltowski, A. J., Vercesi, A. E., Rhee, S. G., & Netto, L. E. S. (2000). Catalases and thioredoxin peroxidase protect Saccharomyces cerevisiae against 'Ca POT.2+'-induced mitochondrial membrane permeabilization and cell death. FEBS Letters, 473, 177-182. doi:10.1016/s0014-5793(00)01526-x
NLM
Kowaltowski AJ, Vercesi AE, Rhee SG, Netto LES. Catalases and thioredoxin peroxidase protect Saccharomyces cerevisiae against 'Ca POT.2+'-induced mitochondrial membrane permeabilization and cell death [Internet]. FEBS Letters. 2000 ; 473 177-182.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/s0014-5793(00)01526-x
Vancouver
Kowaltowski AJ, Vercesi AE, Rhee SG, Netto LES. Catalases and thioredoxin peroxidase protect Saccharomyces cerevisiae against 'Ca POT.2+'-induced mitochondrial membrane permeabilization and cell death [Internet]. FEBS Letters. 2000 ; 473 177-182.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/s0014-5793(00)01526-x
Artigo de periodico
Sex chromosome evolution in fish: the formation of the neo-Y chromosome in Eigenmannia (Gymnotiformes) (2000)
Almeida-Toledo, Lurdes Foresti de; Foresti, Fausto; Daniel, Maria de Fátima Zambelli; Toledo Filho, Sílvio de Almeida
Source: Chromosoma. Unidade: IB
Assunto: PEIXES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ALMEIDA-TOLEDO, Lurdes Foresti de et al. Sex chromosome evolution in fish: the formation of the neo-Y chromosome in Eigenmannia (Gymnotiformes). Chromosoma, v. 109, p. 197-200, 2000Tradução . . Disponível em: https://doi.org/10.1007/s004120050428. Acesso em: 01 nov. 2024.
APA
Almeida-Toledo, L. F. de, Foresti, F., Daniel, M. de F. Z., & Toledo Filho, S. de A. (2000). Sex chromosome evolution in fish: the formation of the neo-Y chromosome in Eigenmannia (Gymnotiformes). Chromosoma, 109, 197-200. doi:10.1007/s004120050428
NLM
Almeida-Toledo LF de, Foresti F, Daniel M de FZ, Toledo Filho S de A. Sex chromosome evolution in fish: the formation of the neo-Y chromosome in Eigenmannia (Gymnotiformes) [Internet]. Chromosoma. 2000 ; 109 197-200.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1007/s004120050428
Vancouver
Almeida-Toledo LF de, Foresti F, Daniel M de FZ, Toledo Filho S de A. Sex chromosome evolution in fish: the formation of the neo-Y chromosome in Eigenmannia (Gymnotiformes) [Internet]. Chromosoma. 2000 ; 109 197-200.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1007/s004120050428
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 01 nov. 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 nov. 01 ]
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 nov. 01 ]
Artigo de periodico
Calculation of recurrence risks for heterogeneous genetic disorders (2000)
Braga, Maria Cristina Célia; Otto, Paulo A ; Frota-Pessoa, Oswaldo
Source: American Journal of Medical Genetics. Unidade: IB
Subjects: ACONSELHAMENTO GENÉTICO, DOENÇAS GENÉTICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BRAGA, Maria Cristina Célia e OTTO, Paulo A e FROTA-PESSOA, Oswaldo. Calculation of recurrence risks for heterogeneous genetic disorders. American Journal of Medical Genetics, v. 95, p. 36-42, 2000Tradução . . Disponível em: https://doi.org/10.1002/1096-8628(20001106)95:1%3C36::aid-ajmg8%3E3.0.co;2-8. Acesso em: 01 nov. 2024.
APA
Braga, M. C. C., Otto, P. A., & Frota-Pessoa, O. (2000). Calculation of recurrence risks for heterogeneous genetic disorders. American Journal of Medical Genetics, 95, 36-42. doi:10.1002/1096-8628(20001106)95:1%3C36::aid-ajmg8%3E3.0.co;2-8
NLM
Braga MCC, Otto PA, Frota-Pessoa O. Calculation of recurrence risks for heterogeneous genetic disorders [Internet]. American Journal of Medical Genetics. 2000 ; 95 36-42.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1002/1096-8628(20001106)95:1%3C36::aid-ajmg8%3E3.0.co;2-8
Vancouver
Braga MCC, Otto PA, Frota-Pessoa O. Calculation of recurrence risks for heterogeneous genetic disorders [Internet]. American Journal of Medical Genetics. 2000 ; 95 36-42.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1002/1096-8628(20001106)95:1%3C36::aid-ajmg8%3E3.0.co;2-8
Artigo de periodico
Collagen XVIII, containing an endogenous inhibitor of angiogenesis and tumor growth, plays a critical role in the maintenance of retinal structure and in neural tube closure (Knobloch syndrome) (2000)
Sertié, Andréa Laurato; Sossi, Vittorio; Camargo, Ana Maria A; Zatz, Mayana ; Brahe, Christina; Passos-Bueno, Maria Rita
Source: Human Molecular Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SERTIÉ, Andréa Laurato et al. Collagen XVIII, containing an endogenous inhibitor of angiogenesis and tumor growth, plays a critical role in the maintenance of retinal structure and in neural tube closure (Knobloch syndrome). Human Molecular Genetics, v. 9, n. 13, p. 2051-2058, 2000Tradução . . Acesso em: 01 nov. 2024.
APA
Sertié, A. L., Sossi, V., Camargo, A. M. A., Zatz, M., Brahe, C., & Passos-Bueno, M. R. (2000). Collagen XVIII, containing an endogenous inhibitor of angiogenesis and tumor growth, plays a critical role in the maintenance of retinal structure and in neural tube closure (Knobloch syndrome). Human Molecular Genetics, 9( 13), 2051-2058.
NLM
Sertié AL, Sossi V, Camargo AMA, Zatz M, Brahe C, Passos-Bueno MR. Collagen XVIII, containing an endogenous inhibitor of angiogenesis and tumor growth, plays a critical role in the maintenance of retinal structure and in neural tube closure (Knobloch syndrome). Human Molecular Genetics. 2000 ; 9( 13): 2051-2058.[citado 2024 nov. 01 ]
Vancouver
Sertié AL, Sossi V, Camargo AMA, Zatz M, Brahe C, Passos-Bueno MR. Collagen XVIII, containing an endogenous inhibitor of angiogenesis and tumor growth, plays a critical role in the maintenance of retinal structure and in neural tube closure (Knobloch syndrome). Human Molecular Genetics. 2000 ; 9( 13): 2051-2058.[citado 2024 nov. 01 ]
Artigo de periodico
Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasia (2000)
Iughetti, Paula; Alonso, Luís Garcia; Wilcox, William; Alonso, Nivaldo
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
IUGHETTI, Paula et al. Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasia. American Journal of Medical Genetics, n. 95, p. 482-491, 2000Tradução . . Disponível em: https://doi.org/10.1002/1096-8628(20001218)95:5%3C482::aid-ajmg14%3E3.0.co;2-x. Acesso em: 01 nov. 2024.
APA
Iughetti, P., Alonso, L. G., Wilcox, W., & Alonso, N. (2000). Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasia. American Journal of Medical Genetics, ( 95), 482-491. doi:10.1002/1096-8628(20001218)95:5%3C482::aid-ajmg14%3E3.0.co;2-x
NLM
Iughetti P, Alonso LG, Wilcox W, Alonso N. Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasia [Internet]. American Journal of Medical Genetics. 2000 ;( 95): 482-491.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1002/1096-8628(20001218)95:5%3C482::aid-ajmg14%3E3.0.co;2-x
Vancouver
Iughetti P, Alonso LG, Wilcox W, Alonso N. Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasia [Internet]. American Journal of Medical Genetics. 2000 ;( 95): 482-491.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1002/1096-8628(20001218)95:5%3C482::aid-ajmg14%3E3.0.co;2-x
Artigo de periodico
Analysis of the disease risk locus DXS1047 polymorphism in brazilian Alzheimer patients (2000)
Nishimura, A L; Oliveira, J. R. M.; Matioli, Sergio Russo ; Brito-Marques, Paulo Roberto; Bahia, Valéria Santoro; Nitrini, Ricardo; Zatz, Mayana
Source: Molecular Psychiatry. Unidades: IB, FM
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NISHIMURA, A L et al. Analysis of the disease risk locus DXS1047 polymorphism in brazilian Alzheimer patients. Molecular Psychiatry, v. 5, p. 563-566, 2000Tradução . . Disponível em: https://doi.org/10.1038/sj.mp.4000767. Acesso em: 01 nov. 2024.
APA
Nishimura, A. L., Oliveira, J. R. M., Matioli, S. R., Brito-Marques, P. R., Bahia, V. S., Nitrini, R., & Zatz, M. (2000). Analysis of the disease risk locus DXS1047 polymorphism in brazilian Alzheimer patients. Molecular Psychiatry, 5, 563-566. doi:10.1038/sj.mp.4000767
NLM
Nishimura AL, Oliveira JRM, Matioli SR, Brito-Marques PR, Bahia VS, Nitrini R, Zatz M. Analysis of the disease risk locus DXS1047 polymorphism in brazilian Alzheimer patients [Internet]. Molecular Psychiatry. 2000 ; 5 563-566.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1038/sj.mp.4000767
Vancouver
Nishimura AL, Oliveira JRM, Matioli SR, Brito-Marques PR, Bahia VS, Nitrini R, Zatz M. Analysis of the disease risk locus DXS1047 polymorphism in brazilian Alzheimer patients [Internet]. Molecular Psychiatry. 2000 ; 5 563-566.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1038/sj.mp.4000767
Artigo de periodico
Sex chromosome evolution in fish. II. Second occurrence of an 'X IND.1''X IND.2'Y sex chromosome system in Gymnotiformes (2000)
Almeida-Toledo, Lurdes Foresti de; Daniel-Silva, Maria de Fátima Zambelli; Lopes, C E; Toledo Filho, Sílvio de Almeida
Source: Chromosome Research. Unidade: IB
Assunto: PEIXES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ALMEIDA-TOLEDO, Lurdes Foresti de et al. Sex chromosome evolution in fish. II. Second occurrence of an 'X IND.1''X IND.2'Y sex chromosome system in Gymnotiformes. Chromosome Research, v. 8, p. 335-340, 2000Tradução . . Acesso em: 01 nov. 2024.
APA
Almeida-Toledo, L. F. de, Daniel-Silva, M. de F. Z., Lopes, C. E., & Toledo Filho, S. de A. (2000). Sex chromosome evolution in fish. II. Second occurrence of an 'X IND.1''X IND.2'Y sex chromosome system in Gymnotiformes. Chromosome Research, 8, 335-340.
NLM
Almeida-Toledo LF de, Daniel-Silva M de FZ, Lopes CE, Toledo Filho S de A. Sex chromosome evolution in fish. II. Second occurrence of an 'X IND.1''X IND.2'Y sex chromosome system in Gymnotiformes. Chromosome Research. 2000 ; 8 335-340.[citado 2024 nov. 01 ]
Vancouver
Almeida-Toledo LF de, Daniel-Silva M de FZ, Lopes CE, Toledo Filho S de A. Sex chromosome evolution in fish. II. Second occurrence of an 'X IND.1''X IND.2'Y sex chromosome system in Gymnotiformes. Chromosome Research. 2000 ; 8 335-340.[citado 2024 nov. 01 ]
Artigo de periodico
High intraspecific karyological conservation in four species of Gymnotus (Pisces: Gymnotiformes) from Southeastern Brazilian basins (1998)
Fernandes-Matioli, Flora Maria de Campos; Marchetto, Maria Carolina Nasser; Almeida-Toledo, Lurdes Foresti de; Toledo Filho, Sílvio de Almeida
Source: Caryologia. Unidade: IB
Assunto: PEIXES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERNANDES-MATIOLI, Flora Maria de Campos et al. High intraspecific karyological conservation in four species of Gymnotus (Pisces: Gymnotiformes) from Southeastern Brazilian basins. Caryologia, v. 51, n. 3-4, p. 221-234, 1998Tradução . . Disponível em: https://doi.org/10.1080/00087114.1998.10797414. Acesso em: 01 nov. 2024.
APA
Fernandes-Matioli, F. M. de C., Marchetto, M. C. N., Almeida-Toledo, L. F. de, & Toledo Filho, S. de A. (1998). High intraspecific karyological conservation in four species of Gymnotus (Pisces: Gymnotiformes) from Southeastern Brazilian basins. Caryologia, 51( 3-4), 221-234. doi:10.1080/00087114.1998.10797414
NLM
Fernandes-Matioli FM de C, Marchetto MCN, Almeida-Toledo LF de, Toledo Filho S de A. High intraspecific karyological conservation in four species of Gymnotus (Pisces: Gymnotiformes) from Southeastern Brazilian basins [Internet]. Caryologia. 1998 ; 51( 3-4): 221-234.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1080/00087114.1998.10797414
Vancouver
Fernandes-Matioli FM de C, Marchetto MCN, Almeida-Toledo LF de, Toledo Filho S de A. High intraspecific karyological conservation in four species of Gymnotus (Pisces: Gymnotiformes) from Southeastern Brazilian basins [Internet]. Caryologia. 1998 ; 51( 3-4): 221-234.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1080/00087114.1998.10797414

USP Schools

ReP

Filtros

Authors

USP affiliated authors

Subjects

Source title

Countries/Territories

Indexado em

Normalized affiliation

Non normalized affiliation