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Trabalho de evento-resumo periodico
Variants within OCA2 and HERC2 genes associated with eye color and iris features in a Brazilian admixed population sample (2019)
Mendes Júnior, Celso Teixeira ; Debortoli, Guilherme ; Parra, E. J.; Marcorin, Letícia ; Pereira, A. L. E.; Fracasso, Nádia Carolina de Aguiar; Oliveira, M. G.; Massaro, Juliana Doblas ; Donadi, Eduardo Antônio ; Simões, Aguinaldo Luiz ; Castelli, Erick C.
Source: European Journal of Human Genetics. Conference titles: European Society of Human Genetics Conference - ESHG. Unidades: FFCLRP, FMRP
Subjects: GENÉTICA MÉDICA, DIAGNÓSTICO PRÉ-NATAL, AGENESIA
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ABNT
MENDES JÚNIOR, Celso Teixeira et al. Variants within OCA2 and HERC2 genes associated with eye color and iris features in a Brazilian admixed population sample. European Journal of Human Genetics. London: Faculdade de Filosofia, Ciências e Letras de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://doi.org/10.1038/s41431-019-0494-2. Acesso em: 27 nov. 2025. , 2019
APA
Mendes Júnior, C. T., Debortoli, G., Parra, E. J., Marcorin, L., Pereira, A. L. E., Fracasso, N. C. de A., et al. (2019). Variants within OCA2 and HERC2 genes associated with eye color and iris features in a Brazilian admixed population sample. European Journal of Human Genetics. London: Faculdade de Filosofia, Ciências e Letras de Ribeirão Preto, Universidade de São Paulo. doi:10.1038/s41431-019-0494-2
NLM
Mendes Júnior CT, Debortoli G, Parra EJ, Marcorin L, Pereira ALE, Fracasso NC de A, Oliveira MG, Massaro JD, Donadi EA, Simões AL, Castelli EC. Variants within OCA2 and HERC2 genes associated with eye color and iris features in a Brazilian admixed population sample [Internet]. European Journal of Human Genetics. 2019 ; 27( 11): 1765.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1038/s41431-019-0494-2
Vancouver
Mendes Júnior CT, Debortoli G, Parra EJ, Marcorin L, Pereira ALE, Fracasso NC de A, Oliveira MG, Massaro JD, Donadi EA, Simões AL, Castelli EC. Variants within OCA2 and HERC2 genes associated with eye color and iris features in a Brazilian admixed population sample [Internet]. European Journal of Human Genetics. 2019 ; 27( 11): 1765.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1038/s41431-019-0494-2
Artigo de periodico
Regulatory variants of FOXG1 in the context of its topological domain organisation (2017)
Mehrjouy, Mana M; Fonseca, Ana Carolina S; Ehmke, Nadja; Paskulin, Giorgio; Novelli, Antonio; Benedicenti, Francesco; Mencarelli, Maria Antonietta; Renieri, Alessandra; Busa, Tiffany; Missirian, Chantal; Hansen, Claus; Abe, Kikue Terada; Speck-Martins, Carlos Eduardo; Vianna-Morgante, Angela M ; Bak, Mads; Tommerup, Niels
Source: European Journal of Human Genetics. Unidade: IB
Subjects: MUTAÇÃO GENÉTICA, CÉLULAS-TRONCO, GENOMAS, CROMOSSOMOS, NEUROGENÉTICA, GENÉTICA MÉDICA
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ABNT
MEHRJOUY, Mana M et al. Regulatory variants of FOXG1 in the context of its topological domain organisation. European Journal of Human Genetics, 2017Tradução . . Disponível em: https://doi.org/10.1038/s41431-017-0011-4. Acesso em: 27 nov. 2025.
APA
Mehrjouy, M. M., Fonseca, A. C. S., Ehmke, N., Paskulin, G., Novelli, A., Benedicenti, F., et al. (2017). Regulatory variants of FOXG1 in the context of its topological domain organisation. European Journal of Human Genetics. doi:10.1038/s41431-017-0011-4
NLM
Mehrjouy MM, Fonseca ACS, Ehmke N, Paskulin G, Novelli A, Benedicenti F, Mencarelli MA, Renieri A, Busa T, Missirian C, Hansen C, Abe KT, Speck-Martins CE, Vianna-Morgante AM, Bak M, Tommerup N. Regulatory variants of FOXG1 in the context of its topological domain organisation [Internet]. European Journal of Human Genetics. 2017 ;[citado 2025 nov. 27 ] Available from: https://doi.org/10.1038/s41431-017-0011-4
Vancouver
Mehrjouy MM, Fonseca ACS, Ehmke N, Paskulin G, Novelli A, Benedicenti F, Mencarelli MA, Renieri A, Busa T, Missirian C, Hansen C, Abe KT, Speck-Martins CE, Vianna-Morgante AM, Bak M, Tommerup N. Regulatory variants of FOXG1 in the context of its topological domain organisation [Internet]. European Journal of Human Genetics. 2017 ;[citado 2025 nov. 27 ] Available from: https://doi.org/10.1038/s41431-017-0011-4
Artigo de periodico
Baraitser-Winter cerebrofrontofacial syndrome: delineation of the spectrum in 42 cases (2015)
Verloes, Alain; Di Donato, Nataliya; Masliah-Planchon, Julien; Jongmans, Marjolijn; Abdul-Raman, Omar A.; Albrecht, Beate; Allanson, Judith; Brunnner, Han; Bertola, Débora; Chassaing, Nicolas; David, Albert; Devriendt, Koen; Eftekhari, Pirayeh; Drouin-Garraud, Valérie; Faravelli, Francesca; Faivre, Laurence; Giuliano, Fabienne; Guion-Almeida, Maria Leine; Juncos, Jorge; Kempers, Marlies; Eker, Hatice Koçak; Lacombe, Didier; Lin, Angela; Mancini, Grazia; Melis, Daniela; Lourenço, Charles Marques; Siu, Victoria Mok; Morin, Gilles; Nezarati, Marjan; Nowaczyk, Malgorzata J. M.; Ramer, Jeanette C.; Osimani, Sara; Philip, Nicole; Pierpont, Mary Ella; Procraccio, Vincent; Zechi-Ceide, Roseli Maria; Rossi, Massimiliano; Rusu, Cristina; Sznajer, Yves; Templin, Ludivine; Uliana, Vera; Klaus, Mirjam; Van Bon, Bregje; Van Ravenswaaij, Conny; Wainer, Bruce; Fry, Andrew E.; Rump, Andreas; Hoischen, Alexander; Drunat, Séverine; Rivière, Jean-Baptiste; Dobyns, William B.; Pilz, Daniela T.
Source: European Journal of Human Genetics. Unidade: HRAC
Subjects: GENÉTICA MÉDICA, ANORMALIDADES CRANIOFACIAIS, MUTAÇÃO GENÉTICA
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ABNT
VERLOES, Alain et al. Baraitser-Winter cerebrofrontofacial syndrome: delineation of the spectrum in 42 cases. European Journal of Human Genetics, v. 23, n. 3, p. 292-301, 2015Tradução . . Disponível em: https://doi.org/10.1038/ejhg.2014.95. Acesso em: 27 nov. 2025.
APA
Verloes, A., Di Donato, N., Masliah-Planchon, J., Jongmans, M., Abdul-Raman, O. A., Albrecht, B., et al. (2015). Baraitser-Winter cerebrofrontofacial syndrome: delineation of the spectrum in 42 cases. European Journal of Human Genetics, 23( 3), 292-301. doi:10.1038/ejhg.2014.95
NLM
Verloes A, Di Donato N, Masliah-Planchon J, Jongmans M, Abdul-Raman OA, Albrecht B, Allanson J, Brunnner H, Bertola D, Chassaing N, David A, Devriendt K, Eftekhari P, Drouin-Garraud V, Faravelli F, Faivre L, Giuliano F, Guion-Almeida ML, Juncos J, Kempers M, Eker HK, Lacombe D, Lin A, Mancini G, Melis D, Lourenço CM, Siu VM, Morin G, Nezarati M, Nowaczyk MJM, Ramer JC, Osimani S, Philip N, Pierpont ME, Procraccio V, Zechi-Ceide RM, Rossi M, Rusu C, Sznajer Y, Templin L, Uliana V, Klaus M, Van Bon B, Van Ravenswaaij C, Wainer B, Fry AE, Rump A, Hoischen A, Drunat S, Rivière J-B, Dobyns WB, Pilz DT. Baraitser-Winter cerebrofrontofacial syndrome: delineation of the spectrum in 42 cases [Internet]. European Journal of Human Genetics. 2015 ; 23( 3): 292-301.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1038/ejhg.2014.95
Vancouver
Verloes A, Di Donato N, Masliah-Planchon J, Jongmans M, Abdul-Raman OA, Albrecht B, Allanson J, Brunnner H, Bertola D, Chassaing N, David A, Devriendt K, Eftekhari P, Drouin-Garraud V, Faravelli F, Faivre L, Giuliano F, Guion-Almeida ML, Juncos J, Kempers M, Eker HK, Lacombe D, Lin A, Mancini G, Melis D, Lourenço CM, Siu VM, Morin G, Nezarati M, Nowaczyk MJM, Ramer JC, Osimani S, Philip N, Pierpont ME, Procraccio V, Zechi-Ceide RM, Rossi M, Rusu C, Sznajer Y, Templin L, Uliana V, Klaus M, Van Bon B, Van Ravenswaaij C, Wainer B, Fry AE, Rump A, Hoischen A, Drunat S, Rivière J-B, Dobyns WB, Pilz DT. Baraitser-Winter cerebrofrontofacial syndrome: delineation of the spectrum in 42 cases [Internet]. European Journal of Human Genetics. 2015 ; 23( 3): 292-301.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1038/ejhg.2014.95
Trabalho de evento-resumo periodico
Genotype-phenotype correlation with ring chromosome 11 (2014)
Martelli, Lucia Regina; Gomes, A. G.; Grangeiro, C. H. P.; Pereira, C. S.; Silva, L. R.; Scarparo, R. M.; Squire, Jeremy Andrew
Source: European Journal of Human Genetics. Conference titles: European Human Genetics Conference. Unidade: FMRP
Subjects: GENÉTICA MÉDICA, CROMOSSOMOS HUMANOS 6-12
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ABNT
MARTELLI, Lucia Regina et al. Genotype-phenotype correlation with ring chromosome 11. European Journal of Human Genetics. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 27 nov. 2025. , 2014
APA
Martelli, L. R., Gomes, A. G., Grangeiro, C. H. P., Pereira, C. S., Silva, L. R., Scarparo, R. M., & Squire, J. A. (2014). Genotype-phenotype correlation with ring chromosome 11. European Journal of Human Genetics. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Martelli LR, Gomes AG, Grangeiro CHP, Pereira CS, Silva LR, Scarparo RM, Squire JA. Genotype-phenotype correlation with ring chromosome 11. European Journal of Human Genetics. 2014 ; 22 451.[citado 2025 nov. 27 ]
Vancouver
Martelli LR, Gomes AG, Grangeiro CHP, Pereira CS, Silva LR, Scarparo RM, Squire JA. Genotype-phenotype correlation with ring chromosome 11. European Journal of Human Genetics. 2014 ; 22 451.[citado 2025 nov. 27 ]
Artigo de periodico
Molecular and clinical delineation of the 17q22 microdeletion phenotype (2013)
Laurell, Tobias; Lundin, Johanna; Anderlid, Britt-Marie; Gorski, Jerome L; Grigelioniene, Giedre; Knight, Samantha J. L; Krepischi, Ana Cristina Victorino ; Nordenskjöld, Agneta; Price, Susan M; Rosenberg, Carla ; Turnpenny, Peter D; Vianna-Morgante, Angela M ; Nordgren, Ann
Source: European Journal of Human Genetics. Unidade: IB
Subjects: FENÓTIPOS, ANOMALIA FACIAL, RETARDO MENTAL, GENÉTICA MÉDICA
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ABNT
LAURELL, Tobias et al. Molecular and clinical delineation of the 17q22 microdeletion phenotype. European Journal of Human Genetics, v. 21, n. 10, p. 1085-1092, 2013Tradução . . Disponível em: https://doi.org/10.1038/ejhg.2012.306. Acesso em: 27 nov. 2025.
APA
Laurell, T., Lundin, J., Anderlid, B. -M., Gorski, J. L., Grigelioniene, G., Knight, S. J. L., et al. (2013). Molecular and clinical delineation of the 17q22 microdeletion phenotype. European Journal of Human Genetics, 21( 10), 1085-1092. doi:10.1038/ejhg.2012.306
NLM
Laurell T, Lundin J, Anderlid B-M, Gorski JL, Grigelioniene G, Knight SJL, Krepischi ACV, Nordenskjöld A, Price SM, Rosenberg C, Turnpenny PD, Vianna-Morgante AM, Nordgren A. Molecular and clinical delineation of the 17q22 microdeletion phenotype [Internet]. European Journal of Human Genetics. 2013 ; 21( 10): 1085-1092.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1038/ejhg.2012.306
Vancouver
Laurell T, Lundin J, Anderlid B-M, Gorski JL, Grigelioniene G, Knight SJL, Krepischi ACV, Nordenskjöld A, Price SM, Rosenberg C, Turnpenny PD, Vianna-Morgante AM, Nordgren A. Molecular and clinical delineation of the 17q22 microdeletion phenotype [Internet]. European Journal of Human Genetics. 2013 ; 21( 10): 1085-1092.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1038/ejhg.2012.306
Artigo de periodico-carta/editorial
Does germ-line deletion of the PIP gene constitute a widespread risk for cancer? [Carta] (2013)
Silva, Amanda G; Krepischi, Ana Cristina Victorino ; Torrezan, Giovana T; Capelli, Leonardo P; Carraro, Dirce M; D'Angelo, Carla S; Koiffmann, Celia Priszkulnik ; Zatz, Mayana ; Naslavsky, Michel ; Masotti, Cibele; Otto, Paulo A ; Achatz, Maria I. W; Mills, Ryan E; Lee, Charles; Pearson, Peter L; Rosenberg, Carla
Source: European Journal of Human Genetics. Unidade: IB
Subjects: GENÉTICA MÉDICA, NEOPLASIAS, PROLACTINA
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ABNT
SILVA, Amanda G et al. Does germ-line deletion of the PIP gene constitute a widespread risk for cancer? [Carta]. European Journal of Human Genetics. London: Instituto de Biociências, Universidade de São Paulo. Disponível em: https://doi.org/10.1038/ejhg.2013.134. Acesso em: 27 nov. 2025. , 2013
APA
Silva, A. G., Krepischi, A. C. V., Torrezan, G. T., Capelli, L. P., Carraro, D. M., D'Angelo, C. S., et al. (2013). Does germ-line deletion of the PIP gene constitute a widespread risk for cancer? [Carta]. European Journal of Human Genetics. London: Instituto de Biociências, Universidade de São Paulo. doi:10.1038/ejhg.2013.134
NLM
Silva AG, Krepischi ACV, Torrezan GT, Capelli LP, Carraro DM, D'Angelo CS, Koiffmann CP, Zatz M, Naslavsky M, Masotti C, Otto PA, Achatz MIW, Mills RE, Lee C, Pearson PL, Rosenberg C. Does germ-line deletion of the PIP gene constitute a widespread risk for cancer? [Carta] [Internet]. European Journal of Human Genetics. 2013 ; 1-3 on-line.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1038/ejhg.2013.134
Vancouver
Silva AG, Krepischi ACV, Torrezan GT, Capelli LP, Carraro DM, D'Angelo CS, Koiffmann CP, Zatz M, Naslavsky M, Masotti C, Otto PA, Achatz MIW, Mills RE, Lee C, Pearson PL, Rosenberg C. Does germ-line deletion of the PIP gene constitute a widespread risk for cancer? [Carta] [Internet]. European Journal of Human Genetics. 2013 ; 1-3 on-line.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1038/ejhg.2013.134
Artigo de periodico
A multi-exonic SPG4 duplication underlies sex-dependent penetrance of hereditary spastic paraplegia in a large brazilian pedigree (2007)
Mitne-Neto, Miguel; Kok, Fernando; Beetz, Christian; Pessoa, André; Bueno, Clarissa; Graciani, Zodja; Martyn, Marcilia; Monteiro, Carlos Bandeira de Mello; Mitne, Guilherme; Hubert, Paulo; Nygren, Anders O. H; Valadares, Marcos; Cerqueira, Antonia Maria Pereira de; Starling, Alessandra; Deufel, Thomas; Zatz, Mayana
Source: European Journal of Human Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
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ABNT
MITNE-NETO, Miguel et al. A multi-exonic SPG4 duplication underlies sex-dependent penetrance of hereditary spastic paraplegia in a large brazilian pedigree. European Journal of Human Genetics, v. 15, n. 12, p. 1276-1279, 2007Tradução . . Disponível em: https://doi.org/10.1038/sj.ejhg.5201924. Acesso em: 27 nov. 2025.
APA
Mitne-Neto, M., Kok, F., Beetz, C., Pessoa, A., Bueno, C., Graciani, Z., et al. (2007). A multi-exonic SPG4 duplication underlies sex-dependent penetrance of hereditary spastic paraplegia in a large brazilian pedigree. European Journal of Human Genetics, 15( 12), 1276-1279. doi:10.1038/sj.ejhg.5201924
NLM
Mitne-Neto M, Kok F, Beetz C, Pessoa A, Bueno C, Graciani Z, Martyn M, Monteiro CB de M, Mitne G, Hubert P, Nygren AOH, Valadares M, Cerqueira AMP de, Starling A, Deufel T, Zatz M. A multi-exonic SPG4 duplication underlies sex-dependent penetrance of hereditary spastic paraplegia in a large brazilian pedigree [Internet]. European Journal of Human Genetics. 2007 ; 15( 12): 1276-1279.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1038/sj.ejhg.5201924
Vancouver
Mitne-Neto M, Kok F, Beetz C, Pessoa A, Bueno C, Graciani Z, Martyn M, Monteiro CB de M, Mitne G, Hubert P, Nygren AOH, Valadares M, Cerqueira AMP de, Starling A, Deufel T, Zatz M. A multi-exonic SPG4 duplication underlies sex-dependent penetrance of hereditary spastic paraplegia in a large brazilian pedigree [Internet]. European Journal of Human Genetics. 2007 ; 15( 12): 1276-1279.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1038/sj.ejhg.5201924
Trabalho de evento-resumo periodico
Y-Chromosome biallelic polyorphisms in Afro-Brazilian populations (2002)
Abe-Sandes, Kiyoko; Silva Júnior, Wilson Araújo da; Zago, Marco Antônio
Source: European Journal of Human Genetics. Conference titles: European Human Genetics Conference. Unidade: FMRP
Assunto: GENÉTICA MÉDICA
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ABNT
ABE-SANDES, Kiyoko e SILVA JÚNIOR, Wilson Araújo da e ZAGO, Marco Antônio. Y-Chromosome biallelic polyorphisms in Afro-Brazilian populations. European Journal of Human Genetics. [S.l.]: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 27 nov. 2025. , 2002
APA
Abe-Sandes, K., Silva Júnior, W. A. da, & Zago, M. A. (2002). Y-Chromosome biallelic polyorphisms in Afro-Brazilian populations. European Journal of Human Genetics. Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Abe-Sandes K, Silva Júnior WA da, Zago MA. Y-Chromosome biallelic polyorphisms in Afro-Brazilian populations. European Journal of Human Genetics. 2002 ; 10 188.[citado 2025 nov. 27 ]
Vancouver
Abe-Sandes K, Silva Júnior WA da, Zago MA. Y-Chromosome biallelic polyorphisms in Afro-Brazilian populations. European Journal of Human Genetics. 2002 ; 10 188.[citado 2025 nov. 27 ]
Trabalho de evento-resumo periodico
Spectral Karyotyping study of three patients with constitutional supernumerary chromossomal markers (2002)
Ramos, Ester Silveira; Martelli, Lúcia Regina; Karaskowa, J.; Huber, J.; Giuliani, L. D. R.; Versiani, Beatriz R.; Machado, Maria Lúcia; Laureano, Lucimar A. F.; Squire, J.
Source: European Journal of Human Genetics. Conference titles: European Human Genetics Conference. Unidade: FMRP
Assunto: GENÉTICA MÉDICA
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ABNT
RAMOS, Ester Silveira et al. Spectral Karyotyping study of three patients with constitutional supernumerary chromossomal markers. European Journal of Human Genetics. [S.l.]: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 27 nov. 2025. , 2002
APA
Ramos, E. S., Martelli, L. R., Karaskowa, J., Huber, J., Giuliani, L. D. R., Versiani, B. R., et al. (2002). Spectral Karyotyping study of three patients with constitutional supernumerary chromossomal markers. European Journal of Human Genetics. Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Ramos ES, Martelli LR, Karaskowa J, Huber J, Giuliani LDR, Versiani BR, Machado ML, Laureano LAF, Squire J. Spectral Karyotyping study of three patients with constitutional supernumerary chromossomal markers. European Journal of Human Genetics. 2002 ; 10 132.[citado 2025 nov. 27 ]
Vancouver
Ramos ES, Martelli LR, Karaskowa J, Huber J, Giuliani LDR, Versiani BR, Machado ML, Laureano LAF, Squire J. Spectral Karyotyping study of three patients with constitutional supernumerary chromossomal markers. European Journal of Human Genetics. 2002 ; 10 132.[citado 2025 nov. 27 ]
Trabalho de evento-resumo periodico
Acute monocytic leukemia and multiple abnormalities in a child with duplication of 1q detected by GTG-banding and SKY (2002)
Baruffi, Marcelo Razera; Scrideli, Carlos Alberto; Squire, J. A.; Karaskowa, J.; Ramos, Ester Silveira; Heck, B.; Tone, Luiz Gonzaga
Source: European Journal of Human Genetics. Conference titles: European Human Genetics Conference 2002. Unidade: FMRP
Subjects: ONCOLOGIA, PEDIATRIA, GENÉTICA MÉDICA
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ABNT
BARUFFI, Marcelo Razera et al. Acute monocytic leukemia and multiple abnormalities in a child with duplication of 1q detected by GTG-banding and SKY. European Journal of Human Genetics. New York: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 27 nov. 2025. , 2002
APA
Baruffi, M. R., Scrideli, C. A., Squire, J. A., Karaskowa, J., Ramos, E. S., Heck, B., & Tone, L. G. (2002). Acute monocytic leukemia and multiple abnormalities in a child with duplication of 1q detected by GTG-banding and SKY. European Journal of Human Genetics. New York: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Baruffi MR, Scrideli CA, Squire JA, Karaskowa J, Ramos ES, Heck B, Tone LG. Acute monocytic leukemia and multiple abnormalities in a child with duplication of 1q detected by GTG-banding and SKY. European Journal of Human Genetics. 2002 ; 10 91 res. P0082.[citado 2025 nov. 27 ]
Vancouver
Baruffi MR, Scrideli CA, Squire JA, Karaskowa J, Ramos ES, Heck B, Tone LG. Acute monocytic leukemia and multiple abnormalities in a child with duplication of 1q detected by GTG-banding and SKY. European Journal of Human Genetics. 2002 ; 10 91 res. P0082.[citado 2025 nov. 27 ]
Trabalho de evento-resumo periodico
Polymorphism of the MUC 1 mucin 60-bp microsatelite is not associated to women infertility nor to embryo implantation failure (2002)
Goulart, Luís Ricardo; Vieria, G. S.; Inácio, J.; Goulart, Isabela Maria Bernardes; Martelli, Lúcia Regina; Franco Júnior, José Gonçalves
Source: European Journal of Human Genetics. Conference titles: European Human Genetics Conference. Unidade: FMRP
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GOULART, Luís Ricardo et al. Polymorphism of the MUC 1 mucin 60-bp microsatelite is not associated to women infertility nor to embryo implantation failure. European Journal of Human Genetics. [S.l.]: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 27 nov. 2025. , 2002
APA
Goulart, L. R., Vieria, G. S., Inácio, J., Goulart, I. M. B., Martelli, L. R., & Franco Júnior, J. G. (2002). Polymorphism of the MUC 1 mucin 60-bp microsatelite is not associated to women infertility nor to embryo implantation failure. European Journal of Human Genetics. Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Goulart LR, Vieria GS, Inácio J, Goulart IMB, Martelli LR, Franco Júnior JG. Polymorphism of the MUC 1 mucin 60-bp microsatelite is not associated to women infertility nor to embryo implantation failure. European Journal of Human Genetics. 2002 ; 10 304.[citado 2025 nov. 27 ]
Vancouver
Goulart LR, Vieria GS, Inácio J, Goulart IMB, Martelli LR, Franco Júnior JG. Polymorphism of the MUC 1 mucin 60-bp microsatelite is not associated to women infertility nor to embryo implantation failure. European Journal of Human Genetics. 2002 ; 10 304.[citado 2025 nov. 27 ]
Trabalho de evento-resumo periodico
Recurrent basque and brailian mutation in LGMD2A (Calpainopathy) brazilian families (2001)
Paula, Flavia de; Viegas, R.; Kai, A.; Moreira, E S; Passos-Bueno, Maria Rita ; Vainzof, Mariz ; Nigro, Vicenzo; Zatz, Mayana
Source: European Journal of Human Genetics. Conference titles: International Congress of Human Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PAULA, Flavia de et al. Recurrent basque and brailian mutation in LGMD2A (Calpainopathy) brazilian families. European Journal of Human Genetics. Basingstoke: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 27 nov. 2025. , 2001
APA
Paula, F. de, Viegas, R., Kai, A., Moreira, E. S., Passos-Bueno, M. R., Vainzof, M., et al. (2001). Recurrent basque and brailian mutation in LGMD2A (Calpainopathy) brazilian families. European Journal of Human Genetics. Basingstoke: Instituto de Biociências, Universidade de São Paulo.
NLM
Paula F de, Viegas R, Kai A, Moreira ES, Passos-Bueno MR, Vainzof M, Nigro V, Zatz M. Recurrent basque and brailian mutation in LGMD2A (Calpainopathy) brazilian families. European Journal of Human Genetics. 2001 ; 9 396.[citado 2025 nov. 27 ]
Vancouver
Paula F de, Viegas R, Kai A, Moreira ES, Passos-Bueno MR, Vainzof M, Nigro V, Zatz M. Recurrent basque and brailian mutation in LGMD2A (Calpainopathy) brazilian families. European Journal of Human Genetics. 2001 ; 9 396.[citado 2025 nov. 27 ]
Trabalho de evento-resumo periodico
Muscular dystrophies; same mutation but different clinical courses? The next challenge (2001)
Zatz, Mayana ; Vainzof, Mariz ; Passos-Bueno, Maria Rita
Source: European Journal of Human Genetics. Conference titles: International Congress of Human Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana e VAINZOF, Mariz e PASSOS-BUENO, Maria Rita. Muscular dystrophies; same mutation but different clinical courses? The next challenge. European Journal of Human Genetics. Basingstoke: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 27 nov. 2025. , 2001
APA
Zatz, M., Vainzof, M., & Passos-Bueno, M. R. (2001). Muscular dystrophies; same mutation but different clinical courses? The next challenge. European Journal of Human Genetics. Basingstoke: Instituto de Biociências, Universidade de São Paulo.
NLM
Zatz M, Vainzof M, Passos-Bueno MR. Muscular dystrophies; same mutation but different clinical courses? The next challenge. European Journal of Human Genetics. 2001 ; 9 68-69.[citado 2025 nov. 27 ]
Vancouver
Zatz M, Vainzof M, Passos-Bueno MR. Muscular dystrophies; same mutation but different clinical courses? The next challenge. European Journal of Human Genetics. 2001 ; 9 68-69.[citado 2025 nov. 27 ]
Trabalho de evento-resumo periodico
Pericentric inversion of chromosome 9 in recurrent reproductive loss (2001)
Martinelli, Lucia Regina; Pereir-Martins, S. R.; Santos, S. A.; Laureano, L. A. F.; Martinez, Alexandre Souto; Franco Junior, J. G.
Source: European Journal of Human Genetics. Conference titles: International Congress of Human Genetics. Unidades: FMRP, FFCLRP
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MARTINELLI, Lucia Regina et al. Pericentric inversion of chromosome 9 in recurrent reproductive loss. European Journal of Human Genetics. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 27 nov. 2025. , 2001
APA
Martinelli, L. R., Pereir-Martins, S. R., Santos, S. A., Laureano, L. A. F., Martinez, A. S., & Franco Junior, J. G. (2001). Pericentric inversion of chromosome 9 in recurrent reproductive loss. European Journal of Human Genetics. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Martinelli LR, Pereir-Martins SR, Santos SA, Laureano LAF, Martinez AS, Franco Junior JG. Pericentric inversion of chromosome 9 in recurrent reproductive loss. European Journal of Human Genetics. 2001 ; 9( supl. 1): 165.[citado 2025 nov. 27 ]
Vancouver
Martinelli LR, Pereir-Martins SR, Santos SA, Laureano LAF, Martinez AS, Franco Junior JG. Pericentric inversion of chromosome 9 in recurrent reproductive loss. European Journal of Human Genetics. 2001 ; 9( supl. 1): 165.[citado 2025 nov. 27 ]
Trabalho de evento-resumo periodico
Protein analysis in autosomal recessive limb-girdle muscular dystrophies (AR-Igmd) (2001)
Vainzof, Mariz ; Moreira, E S; Paula, Flavia de; Pavanello, Rita de Cássia M; Passos-Bueno, Maria Rita ; Zatz, Mayana
Source: European Journal of Human Genetics. Conference titles: International Congress of Human Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VAINZOF, Mariz et al. Protein analysis in autosomal recessive limb-girdle muscular dystrophies (AR-Igmd). European Journal of Human Genetics. Basingstoke: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 27 nov. 2025. , 2001
APA
Vainzof, M., Moreira, E. S., Paula, F. de, Pavanello, R. de C. M., Passos-Bueno, M. R., & Zatz, M. (2001). Protein analysis in autosomal recessive limb-girdle muscular dystrophies (AR-Igmd). European Journal of Human Genetics. Basingstoke: Instituto de Biociências, Universidade de São Paulo.
NLM
Vainzof M, Moreira ES, Paula F de, Pavanello R de CM, Passos-Bueno MR, Zatz M. Protein analysis in autosomal recessive limb-girdle muscular dystrophies (AR-Igmd). European Journal of Human Genetics. 2001 ; 9 396.[citado 2025 nov. 27 ]
Vancouver
Vainzof M, Moreira ES, Paula F de, Pavanello R de CM, Passos-Bueno MR, Zatz M. Protein analysis in autosomal recessive limb-girdle muscular dystrophies (AR-Igmd). European Journal of Human Genetics. 2001 ; 9 396.[citado 2025 nov. 27 ]

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