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Artigo de periodico
ESR1 polymorphism (rs2234693) influences femoral bone mass in patients with Turner syndrome (2019)
Scalco, Renata C; Trarbach, Ericka B; Albuquerque, Edoarda V. A; Homma, Thais K; Inoue-Lima, Thais H; Nishi, Mirian Y; Mendonça, Berenice Bilharinho de ; Jorge, Alexander Augusto de Lima
Source: Endocrine connections. Unidade: FM
Subjects: TRANSTORNOS DO DESENVOLVIMENTO SEXUAL, POLIMORFISMO, DENSIDADE ÓSSEA, MAMA, ÚTERO, TERAPIA DE REPOSIÇÃO DE ESTRÓGENOS, RECEPTORES DE ESTEROIDES
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ABNT
SCALCO, Renata C et al. ESR1 polymorphism (rs2234693) influences femoral bone mass in patients with Turner syndrome. Endocrine connections, v. 8, n. 11, p. 1513-1519, 2019Tradução . . Disponível em: https://doi.org/10.1530/EC-19-0398. Acesso em: 05 nov. 2024.
APA
Scalco, R. C., Trarbach, E. B., Albuquerque, E. V. A., Homma, T. K., Inoue-Lima, T. H., Nishi, M. Y., et al. (2019). ESR1 polymorphism (rs2234693) influences femoral bone mass in patients with Turner syndrome. Endocrine connections, 8( 11), 1513-1519. doi:10.1530/EC-19-0398
NLM
Scalco RC, Trarbach EB, Albuquerque EVA, Homma TK, Inoue-Lima TH, Nishi MY, Mendonça BB de, Jorge AA de L. ESR1 polymorphism (rs2234693) influences femoral bone mass in patients with Turner syndrome [Internet]. Endocrine connections. 2019 ; 8( 11): 1513-1519.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1530/EC-19-0398
Vancouver
Scalco RC, Trarbach EB, Albuquerque EVA, Homma TK, Inoue-Lima TH, Nishi MY, Mendonça BB de, Jorge AA de L. ESR1 polymorphism (rs2234693) influences femoral bone mass in patients with Turner syndrome [Internet]. Endocrine connections. 2019 ; 8( 11): 1513-1519.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1530/EC-19-0398
Artigo de periodico
Biallelic and monoallelic ESR2 variants associated with 46,XY disorders of sex development (2018)
Baetens, Dorien; Mendonça, Berenice Bilharinho de
Source: Genetics in medicine. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, POLIMORFISMO, RECEPTORES HORMONAIS, SEQUENCIAMENTO GENÉTICO
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ABNT
BAETENS, Dorien e MENDONÇA, Berenice Bilharinho de. Biallelic and monoallelic ESR2 variants associated with 46,XY disorders of sex development. Genetics in medicine, v. 20, n. 7, p. 717-727, 2018Tradução . . Disponível em: https://doi.org/10.1038/gim.2017.163. Acesso em: 05 nov. 2024.
APA
Baetens, D., & Mendonça, B. B. de. (2018). Biallelic and monoallelic ESR2 variants associated with 46,XY disorders of sex development. Genetics in medicine, 20( 7), 717-727. doi:10.1038/gim.2017.163
NLM
Baetens D, Mendonça BB de. Biallelic and monoallelic ESR2 variants associated with 46,XY disorders of sex development [Internet]. Genetics in medicine. 2018 ; 20( 7): 717-727.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1038/gim.2017.163
Vancouver
Baetens D, Mendonça BB de. Biallelic and monoallelic ESR2 variants associated with 46,XY disorders of sex development [Internet]. Genetics in medicine. 2018 ; 20( 7): 717-727.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1038/gim.2017.163
Artigo de periodico
Genetic Predictors of Long-Term Response to Growth Hormone (GH) Therapy in Children With GH Deficiency and Turner Syndrome: the influence of a SOCS2 polymorphism (2014)
Braz, Adriana F.; Costalonga, Everlayny F.; Trarbach, Ericka B.; Scalco, Renata C.; Malaquias, Alexsandra C.; Guerra-Junior, Gil; Antonini, Sonir Roberto Rauber; Mendonça, Berenice Bilharinho de; Arnhold, Ivo J. P.; Jorge, Alexander Augusto de Lima
Source: Journal of clinical endocrinology and metabolism. Unidades: FMRP, FM
Subjects: CRIANÇAS, POLIMORFISMO, CIÊNCIA (TERAPIA)
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ABNT
BRAZ, Adriana F. et al. Genetic Predictors of Long-Term Response to Growth Hormone (GH) Therapy in Children With GH Deficiency and Turner Syndrome: the influence of a SOCS2 polymorphism. Journal of clinical endocrinology and metabolism, v. 99, n. 9, p. E1808-E1813, 2014Tradução . . Disponível em: https://doi.org/10.1210/jc.2014-1744. Acesso em: 05 nov. 2024.
APA
Braz, A. F., Costalonga, E. F., Trarbach, E. B., Scalco, R. C., Malaquias, A. C., Guerra-Junior, G., et al. (2014). Genetic Predictors of Long-Term Response to Growth Hormone (GH) Therapy in Children With GH Deficiency and Turner Syndrome: the influence of a SOCS2 polymorphism. Journal of clinical endocrinology and metabolism, 99( 9), E1808-E1813. doi:10.1210/jc.2014-1744
NLM
Braz AF, Costalonga EF, Trarbach EB, Scalco RC, Malaquias AC, Guerra-Junior G, Antonini SRR, Mendonça BB de, Arnhold IJP, Jorge AA de L. Genetic Predictors of Long-Term Response to Growth Hormone (GH) Therapy in Children With GH Deficiency and Turner Syndrome: the influence of a SOCS2 polymorphism [Internet]. Journal of clinical endocrinology and metabolism. 2014 ; 99( 9): E1808-E1813.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1210/jc.2014-1744
Vancouver
Braz AF, Costalonga EF, Trarbach EB, Scalco RC, Malaquias AC, Guerra-Junior G, Antonini SRR, Mendonça BB de, Arnhold IJP, Jorge AA de L. Genetic Predictors of Long-Term Response to Growth Hormone (GH) Therapy in Children With GH Deficiency and Turner Syndrome: the influence of a SOCS2 polymorphism [Internet]. Journal of clinical endocrinology and metabolism. 2014 ; 99( 9): E1808-E1813.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1210/jc.2014-1744
Trabalho de evento-resumo periodico
Polymorphism rs8081612 in the mitogen-activated protein 3 kinase 3 (MAP3K3) gene is associated with children height ina brazilian cohort (2013)
Fontenele, Eveline Gadelha Pereira; d'Alva, Catarina B.; Pinheiro, Daniel P.; Trarbarch,Ericka; Mendonça, Berenice Bilharinho de; Moraes, Maria Elisabete A.; Jorge, Alexander Augusto de Lima
Source: Hormone Research in Paediatrics. Conference titles: European Society for Paediatric Endocrinology (ESPE)/ Joint Meeting. Unidade: FM
Subjects: GENES (ANÁLISE), PESOS E MEDIDAS CORPORAIS, POLIMORFISMO, CRIANÇAS, BRASIL
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ABNT
FONTENELE, Eveline Gadelha Pereira et al. Polymorphism rs8081612 in the mitogen-activated protein 3 kinase 3 (MAP3K3) gene is associated with children height ina brazilian cohort. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1159/000353762. Acesso em: 05 nov. 2024. , 2013
APA
Fontenele, E. G. P., d'Alva, C. B., Pinheiro, D. P., Trarbarch, E., Mendonça, B. B. de, Moraes, M. E. A., & Jorge, A. A. de L. (2013). Polymorphism rs8081612 in the mitogen-activated protein 3 kinase 3 (MAP3K3) gene is associated with children height ina brazilian cohort. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. doi:10.1159/000353762
NLM
Fontenele EGP, d'Alva CB, Pinheiro DP, Trarbarch E, Mendonça BB de, Moraes MEA, Jorge AA de L. Polymorphism rs8081612 in the mitogen-activated protein 3 kinase 3 (MAP3K3) gene is associated with children height ina brazilian cohort [Internet]. Hormone Research in Paediatrics. 2013 ; 80 295.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1159/000353762
Vancouver
Fontenele EGP, d'Alva CB, Pinheiro DP, Trarbarch E, Mendonça BB de, Moraes MEA, Jorge AA de L. Polymorphism rs8081612 in the mitogen-activated protein 3 kinase 3 (MAP3K3) gene is associated with children height ina brazilian cohort [Internet]. Hormone Research in Paediatrics. 2013 ; 80 295.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1159/000353762
Trabalho de evento-resumo periodico
The presence of clitoomegaly in nonclassical form of 21-hydroxylase deficiency is modulated by the cag polymorphic tract of androgen receptor gene (2010)
Moura, V O; Pacheco, M; Kaupert, L; Gomes, L G; Marcondes, J A M; Mendonça, Berenice Bilharinho de; Bachega, Tânia Aparecida Sartori Sanchez
Source: Clinics. Conference titles: Simpósio "Avanços em Pesquisas Médicas dos Laboratórios de Investigação Médica do Hospital das Clínicas da FMUSP". Unidade: FM
Subjects: HIDROXILASE (DEFICIÊNCIA), POLIMORFISMO, ANDRÓGENOS, RECEPTORES, GENES (ANÁLISE), RESUMOS (EVENTOS)
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ABNT
MOURA, V O et al. The presence of clitoomegaly in nonclassical form of 21-hydroxylase deficiency is modulated by the cag polymorphic tract of androgen receptor gene. Clinics. São Paulo: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 05 nov. 2024. , 2010
APA
Moura, V. O., Pacheco, M., Kaupert, L., Gomes, L. G., Marcondes, J. A. M., Mendonça, B. B. de, & Bachega, T. A. S. S. (2010). The presence of clitoomegaly in nonclassical form of 21-hydroxylase deficiency is modulated by the cag polymorphic tract of androgen receptor gene. Clinics. São Paulo: Faculdade de Medicina, Universidade de São Paulo.
NLM
Moura VO, Pacheco M, Kaupert L, Gomes LG, Marcondes JAM, Mendonça BB de, Bachega TASS. The presence of clitoomegaly in nonclassical form of 21-hydroxylase deficiency is modulated by the cag polymorphic tract of androgen receptor gene. Clinics. 2010 ; 65 S70.[citado 2024 nov. 05 ]
Vancouver
Moura VO, Pacheco M, Kaupert L, Gomes LG, Marcondes JAM, Mendonça BB de, Bachega TASS. The presence of clitoomegaly in nonclassical form of 21-hydroxylase deficiency is modulated by the cag polymorphic tract of androgen receptor gene. Clinics. 2010 ; 65 S70.[citado 2024 nov. 05 ]
Artigo de periodico
TCF21 gene analysis in brazilian patients with 46,XY and 46,XX disorders of gonadal development (2007)
Gomes, C.; Domenice, S.; Santos, M.; Arnhold, I.; Mendonça, Berenice Bilharinho de; Costa, E.
Source: Hormone research. Conference titles: Annual meeting of the sociedad latino-americana de endocrinología pediátrica - SLEP. Unidade: FM
Subjects: TÉCNICAS DE DIAGNÓSTICO E PROCEDIMENTOS, MUTAÇÃO GENÉTICA (ETIOLOGIA), POLIMORFISMO
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ABNT
GOMES, C. et al. TCF21 gene analysis in brazilian patients with 46,XY and 46,XX disorders of gonadal development. Hormone research, v. 68, p. 12, 2007Tradução . . Acesso em: 05 nov. 2024.
APA
Gomes, C., Domenice, S., Santos, M., Arnhold, I., Mendonça, B. B. de, & Costa, E. (2007). TCF21 gene analysis in brazilian patients with 46,XY and 46,XX disorders of gonadal development. Hormone research, 68, 12.
NLM
Gomes C, Domenice S, Santos M, Arnhold I, Mendonça BB de, Costa E. TCF21 gene analysis in brazilian patients with 46,XY and 46,XX disorders of gonadal development. Hormone research. 2007 ; 68 12.[citado 2024 nov. 05 ]
Vancouver
Gomes C, Domenice S, Santos M, Arnhold I, Mendonça BB de, Costa E. TCF21 gene analysis in brazilian patients with 46,XY and 46,XX disorders of gonadal development. Hormone research. 2007 ; 68 12.[citado 2024 nov. 05 ]
Artigo de periodico
Presence of several polyadenylation signal polymorphisms in IGF1 gene of children born small for gestational age (SGA) with and without postnatal catch-up growth (2007)
Coutinho, D.; Coletta, R.; Costa, E.; Boguszewski, M.; Pachi, P.; Damiani, D.; Arnhold, I.; Mendonça, Berenice Bilharinho de; Jorge, A.
Source: Hormone research. Conference titles: Annual meeting of the sociedad latino-americana de endocrinología pediátrica - SLEP. Unidade: FM
Subjects: POLIMORFISMO, ALELOPATIA, CRIANÇAS, RECÉM-NASCIDO PEQUENO PARA IDADE GESTACIONAL
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ABNT
COUTINHO, D. et al. Presence of several polyadenylation signal polymorphisms in IGF1 gene of children born small for gestational age (SGA) with and without postnatal catch-up growth. Hormone research, v. 68, p. 8, 2007Tradução . . Acesso em: 05 nov. 2024.
APA
Coutinho, D., Coletta, R., Costa, E., Boguszewski, M., Pachi, P., Damiani, D., et al. (2007). Presence of several polyadenylation signal polymorphisms in IGF1 gene of children born small for gestational age (SGA) with and without postnatal catch-up growth. Hormone research, 68, 8.
NLM
Coutinho D, Coletta R, Costa E, Boguszewski M, Pachi P, Damiani D, Arnhold I, Mendonça BB de, Jorge A. Presence of several polyadenylation signal polymorphisms in IGF1 gene of children born small for gestational age (SGA) with and without postnatal catch-up growth. Hormone research. 2007 ; 68 8.[citado 2024 nov. 05 ]
Vancouver
Coutinho D, Coletta R, Costa E, Boguszewski M, Pachi P, Damiani D, Arnhold I, Mendonça BB de, Jorge A. Presence of several polyadenylation signal polymorphisms in IGF1 gene of children born small for gestational age (SGA) with and without postnatal catch-up growth. Hormone research. 2007 ; 68 8.[citado 2024 nov. 05 ]
Artigo de periodico
Influence of GH receptor exon 3 polymorphism on the IGF-I response to variable GH doses during treatment of severe GH deficiency (2007)
Marchisotti, Frederico; Jorge, Alexander; Montenegro, Luciana; Berger, Karina; Mendonça, Berenice Bilharinho de; Arnhold, Ivo
Source: Hormone research. Conference titles: European society for paediatric endocrinology - ESPE. Unidade: FM
Subjects: POLIMORFISMO, HORMÔNIO DO CRESCIMENTO (DEFICIÊNCIA; TERAPIA), PROCESSOS PATOLÓGICOS
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ABNT
MARCHISOTTI, Frederico et al. Influence of GH receptor exon 3 polymorphism on the IGF-I response to variable GH doses during treatment of severe GH deficiency. Hormone research, v. 68, p. 139, 2007Tradução . . Acesso em: 05 nov. 2024.
APA
Marchisotti, F., Jorge, A., Montenegro, L., Berger, K., Mendonça, B. B. de, & Arnhold, I. (2007). Influence of GH receptor exon 3 polymorphism on the IGF-I response to variable GH doses during treatment of severe GH deficiency. Hormone research, 68, 139.
NLM
Marchisotti F, Jorge A, Montenegro L, Berger K, Mendonça BB de, Arnhold I. Influence of GH receptor exon 3 polymorphism on the IGF-I response to variable GH doses during treatment of severe GH deficiency. Hormone research. 2007 ; 68 139.[citado 2024 nov. 05 ]
Vancouver
Marchisotti F, Jorge A, Montenegro L, Berger K, Mendonça BB de, Arnhold I. Influence of GH receptor exon 3 polymorphism on the IGF-I response to variable GH doses during treatment of severe GH deficiency. Hormone research. 2007 ; 68 139.[citado 2024 nov. 05 ]
Artigo de periodico
Found in children with idiopathic short stature and NS-associated signs (2007)
Ferreira, L.; Montenegro, L.; Arnhold, I.; Mendonça, Berenice Bilharinho de; Jorge, A.
Source: Hormone research. Conference titles: Annual meeting of the sociedad latino-americana de endocrinología pediátrica - SLEP. Unidade: FM
Subjects: POLIMORFISMO, PESO-ESTATURA, CRIANÇAS, MUTAÇÃO GENÉTICA
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ABNT
FERREIRA, L. et al. Found in children with idiopathic short stature and NS-associated signs. Hormone research, v. 68, p. 10, 2007Tradução . . Acesso em: 05 nov. 2024.
APA
Ferreira, L., Montenegro, L., Arnhold, I., Mendonça, B. B. de, & Jorge, A. (2007). Found in children with idiopathic short stature and NS-associated signs. Hormone research, 68, 10.
NLM
Ferreira L, Montenegro L, Arnhold I, Mendonça BB de, Jorge A. Found in children with idiopathic short stature and NS-associated signs. Hormone research. 2007 ; 68 10.[citado 2024 nov. 05 ]
Vancouver
Ferreira L, Montenegro L, Arnhold I, Mendonça BB de, Jorge A. Found in children with idiopathic short stature and NS-associated signs. Hormone research. 2007 ; 68 10.[citado 2024 nov. 05 ]
Trabalho de evento-resumo
The single nucleotide polymorphism at codon 72 of the P53 protein ins not associated with adrenocortical tumorigenesis (2006)
Pinto, Emilia M.; Fragoso, Maria Candida B. V.; Mendonça, Berenice Bilharinho de; Latronio, Ana Claudia
Source: Resumos. Conference titles: ENDO 06 - Annual Meeting the endocrine society's. Unidade: FM
Subjects: POLIMORFISMO, GLÂNDULAS SUPRARRENAIS, PROTEÍNAS, RESUMOS (CONGRESSOS)
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ABNT
PINTO, Emilia M. et al. The single nucleotide polymorphism at codon 72 of the P53 protein ins not associated with adrenocortical tumorigenesis. 2006, Anais.. Boston: Faculdade de Medicina, Universidade de São Paulo, 2006. . Acesso em: 05 nov. 2024.
APA
Pinto, E. M., Fragoso, M. C. B. V., Mendonça, B. B. de, & Latronio, A. C. (2006). The single nucleotide polymorphism at codon 72 of the P53 protein ins not associated with adrenocortical tumorigenesis. In Resumos. Boston: Faculdade de Medicina, Universidade de São Paulo.
NLM
Pinto EM, Fragoso MCBV, Mendonça BB de, Latronio AC. The single nucleotide polymorphism at codon 72 of the P53 protein ins not associated with adrenocortical tumorigenesis. Resumos. 2006 ;[citado 2024 nov. 05 ]
Vancouver
Pinto EM, Fragoso MCBV, Mendonça BB de, Latronio AC. The single nucleotide polymorphism at codon 72 of the P53 protein ins not associated with adrenocortical tumorigenesis. Resumos. 2006 ;[citado 2024 nov. 05 ]
Trabalho de evento-resumo
Allelic variantions of the LHX4 gene in patients with hypopituitarism and ectopic neurohypophysis (2004)
Melo, Maria E; Marui, Suemi; Gomes, Miriam C; Arnhold, Ivo J; Mendonça, Berenice Bilharinho de; Knopfelmacher, Mirta
Source: Program and Abstracts. Conference titles: ENDO 2004: The Endocrine Society's Annual Meeting. Unidade: FM
Subjects: DIFERENCIAÇÃO CELULCAR, MUTAÇÃO GENÉTICA, POLIMORFISMO, HIPÓFISE (ANORMALIDADES)
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ABNT
MELO, Maria E et al. Allelic variantions of the LHX4 gene in patients with hypopituitarism and ectopic neurohypophysis. 2004, Anais.. New Orleans: Faculdade de Medicina, Universidade de São Paulo, 2004. . Acesso em: 05 nov. 2024.
APA
Melo, M. E., Marui, S., Gomes, M. C., Arnhold, I. J., Mendonça, B. B. de, & Knopfelmacher, M. (2004). Allelic variantions of the LHX4 gene in patients with hypopituitarism and ectopic neurohypophysis. In Program and Abstracts. New Orleans: Faculdade de Medicina, Universidade de São Paulo.
NLM
Melo ME, Marui S, Gomes MC, Arnhold IJ, Mendonça BB de, Knopfelmacher M. Allelic variantions of the LHX4 gene in patients with hypopituitarism and ectopic neurohypophysis. Program and Abstracts. 2004 ;[citado 2024 nov. 05 ]
Vancouver
Melo ME, Marui S, Gomes MC, Arnhold IJ, Mendonça BB de, Knopfelmacher M. Allelic variantions of the LHX4 gene in patients with hypopituitarism and ectopic neurohypophysis. Program and Abstracts. 2004 ;[citado 2024 nov. 05 ]
Trabalho de evento-resumo
Evidence for a founder effect of the R337H mutation of p53 in brazilian patients with adrenocortical tumors (2004)
Pinto, Emilia M; Billerbeck, Ana Elisa C; Fragoso, Maria Candida B. V; Domenice, Sorahia; Mendonça, Berenice Bilharinho de; Latronico, Ana Claudia
Source: Program and Abstracts. Conference titles: ENDO 2004: The Endocrine Society's Annual Meeting. Unidade: FM
Subjects: BIOMARCADORES, MUTAÇÃO GENÉTICA, POLIMORFISMO, BRASILEIROS
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ABNT
PINTO, Emilia M et al. Evidence for a founder effect of the R337H mutation of p53 in brazilian patients with adrenocortical tumors. 2004, Anais.. New Orleans: Faculdade de Medicina, Universidade de São Paulo, 2004. . Acesso em: 05 nov. 2024.
APA
Pinto, E. M., Billerbeck, A. E. C., Fragoso, M. C. B. V., Domenice, S., Mendonça, B. B. de, & Latronico, A. C. (2004). Evidence for a founder effect of the R337H mutation of p53 in brazilian patients with adrenocortical tumors. In Program and Abstracts. New Orleans: Faculdade de Medicina, Universidade de São Paulo.
NLM
Pinto EM, Billerbeck AEC, Fragoso MCBV, Domenice S, Mendonça BB de, Latronico AC. Evidence for a founder effect of the R337H mutation of p53 in brazilian patients with adrenocortical tumors. Program and Abstracts. 2004 ;[citado 2024 nov. 05 ]
Vancouver
Pinto EM, Billerbeck AEC, Fragoso MCBV, Domenice S, Mendonça BB de, Latronico AC. Evidence for a founder effect of the R337H mutation of p53 in brazilian patients with adrenocortical tumors. Program and Abstracts. 2004 ;[citado 2024 nov. 05 ]
Trabalho de evento-resumo
No evidence of a role for activating mutations and polymorphisms of the FSH receptor in the pathogenesis of iatrogenic ovarian hyperstimulation syndrome (2004)
d'Alva, Catarina B; Serafini, Paulo; Motta, Eduardo; Koherk, Maria Beatriz F; Latronico, Ana Claudia; Mendonça, Berenice Bilharinho de
Source: Program and Abstracts. Conference titles: ENDO 2004: The Endocrine Society's Annual Meeting. Unidade: FM
Subjects: FERTILIZAÇÃO (TERAPIA), MUTAÇÃO GENÉTICA, POLIMORFISMO, OVÁRIO (FISIOPATOLOGIA)
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ABNT
D'ALVA, Catarina B et al. No evidence of a role for activating mutations and polymorphisms of the FSH receptor in the pathogenesis of iatrogenic ovarian hyperstimulation syndrome. 2004, Anais.. New Orleans: Faculdade de Medicina, Universidade de São Paulo, 2004. . Acesso em: 05 nov. 2024.
APA
d'Alva, C. B., Serafini, P., Motta, E., Koherk, M. B. F., Latronico, A. C., & Mendonça, B. B. de. (2004). No evidence of a role for activating mutations and polymorphisms of the FSH receptor in the pathogenesis of iatrogenic ovarian hyperstimulation syndrome. In Program and Abstracts. New Orleans: Faculdade de Medicina, Universidade de São Paulo.
NLM
d'Alva CB, Serafini P, Motta E, Koherk MBF, Latronico AC, Mendonça BB de. No evidence of a role for activating mutations and polymorphisms of the FSH receptor in the pathogenesis of iatrogenic ovarian hyperstimulation syndrome. Program and Abstracts. 2004 ;[citado 2024 nov. 05 ]
Vancouver
d'Alva CB, Serafini P, Motta E, Koherk MBF, Latronico AC, Mendonça BB de. No evidence of a role for activating mutations and polymorphisms of the FSH receptor in the pathogenesis of iatrogenic ovarian hyperstimulation syndrome. Program and Abstracts. 2004 ;[citado 2024 nov. 05 ]
Trabalho de evento-resumo
Allele frequencydistribution of sixteen polymorfic loci in a Brazilian population sample (2003)
Soares-Vieira, J. A.; Billerbeck, A. E. C.; Pinto, E. M.; Iwamura, E. S. M.; Mendonça, Berenice Bilharinho de; Muñoz, Daniel Romero; Otto, Paulo A
Source: Resumos. Conference titles: Simpósio. Unidade: FM
Subjects: POLIMORFISMO, GENÓTIPOS, DNA, CAUCÁSIOS, NEGROS
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ABNT
SOARES-VIEIRA, J. A. et al. Allele frequencydistribution of sixteen polymorfic loci in a Brazilian population sample. 2003, Anais.. São Paulo: Faculdade de Medicina, Universidade de São Paulo, 2003. . Acesso em: 05 nov. 2024.
APA
Soares-Vieira, J. A., Billerbeck, A. E. C., Pinto, E. M., Iwamura, E. S. M., Mendonça, B. B. de, Muñoz, D. R., & Otto, P. A. (2003). Allele frequencydistribution of sixteen polymorfic loci in a Brazilian population sample. In Resumos. São Paulo: Faculdade de Medicina, Universidade de São Paulo.
NLM
Soares-Vieira JA, Billerbeck AEC, Pinto EM, Iwamura ESM, Mendonça BB de, Muñoz DR, Otto PA. Allele frequencydistribution of sixteen polymorfic loci in a Brazilian population sample. Resumos. 2003 ;[citado 2024 nov. 05 ]
Vancouver
Soares-Vieira JA, Billerbeck AEC, Pinto EM, Iwamura ESM, Mendonça BB de, Muñoz DR, Otto PA. Allele frequencydistribution of sixteen polymorfic loci in a Brazilian population sample. Resumos. 2003 ;[citado 2024 nov. 05 ]

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