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Artigo de periodico
Phenotypic and mutational spectrum of ROR2-related Robinow syndrome (2022)
Lima, Ariadne R.; Ferreira, Barbara M.; Zhang, Chaofan; Jolly, Angad; Du, Haowei ; White, Janson J.; Dawood, Moez; Lins, Tulio C.; Chiabai, Marcela A.; van Beusekom, Ellen; Cordoba, Mara S.; Rosa, Erica C. C. Caldas; Kayserili, Hulya; Kimonis, Virginia; Wu, Erica; Mellado, Cecilia; Aggarwal, Vineet; Richieri-Costa, Antonio ; Brunoni, Décio; Canó, Talyta M.; Jorge, Alexander A. L. ; Kim, Chong Ae ; Honjo, Rachel ; Bertola, Débora R. ; Dandalo-Girardi, Raissa M.; Bayram, Yavuz; Gezdirici, Alper; Yilmaz-Gulec, Elif; Gumus, Evren; Yilmaz, Gülay C.; Okamoto, Nobuhiko ; Ohashi, Hirofumi; Coban–Akdemir, Zeynep; Mitani, Tadahiro; Jhangiani, Shalini N.; Muzny, Donna M.; Regattieri, Neysa A. P. ; Pogue, Robert ; Pereira, Rinaldo W.; Otto, Paulo A ; Gibbs, Richard A.; Ali, Bassam R.; van Bokhoven, Hans; Brunner, Han G.; Sutton, V. Reid; Lupski, James R. ; Vianna-Morgante, Angela M ; Carvalho, Claudia M. B. ; Mazzeu, Juliana F.
Source: Human Mutation. Unidades: HRAC, FM, IB
Subjects: FENÓTIPOS, MORFOLOGIA (ANATOMIA), SEQUENCIAMENTO GENÉTICO
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ABNT
LIMA, Ariadne R. et al. Phenotypic and mutational spectrum of ROR2-related Robinow syndrome. Human Mutation, v. 43, n. 7, p. 900-918, 2022Tradução . . Disponível em: https://doi.org/10.1002/humu.24375. Acesso em: 03 jul. 2024.
APA
Lima, A. R., Ferreira, B. M., Zhang, C., Jolly, A., Du, H., White, J. J., et al. (2022). Phenotypic and mutational spectrum of ROR2-related Robinow syndrome. Human Mutation, 43( 7), 900-918. doi:10.1002/humu.24375
NLM
Lima AR, Ferreira BM, Zhang C, Jolly A, Du H, White JJ, Dawood M, Lins TC, Chiabai MA, van Beusekom E, Cordoba MS, Rosa ECCC, Kayserili H, Kimonis V, Wu E, Mellado C, Aggarwal V, Richieri-Costa A, Brunoni D, Canó TM, Jorge AAL, Kim CA, Honjo R, Bertola DR, Dandalo-Girardi RM, Bayram Y, Gezdirici A, Yilmaz-Gulec E, Gumus E, Yilmaz GC, Okamoto N, Ohashi H, Coban–Akdemir Z, Mitani T, Jhangiani SN, Muzny DM, Regattieri NAP, Pogue R, Pereira RW, Otto PA, Gibbs RA, Ali BR, van Bokhoven H, Brunner HG, Sutton VR, Lupski JR, Vianna-Morgante AM, Carvalho CMB, Mazzeu JF. Phenotypic and mutational spectrum of ROR2-related Robinow syndrome [Internet]. Human Mutation. 2022 ; 43( 7): 900-918.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1002/humu.24375
Vancouver
Lima AR, Ferreira BM, Zhang C, Jolly A, Du H, White JJ, Dawood M, Lins TC, Chiabai MA, van Beusekom E, Cordoba MS, Rosa ECCC, Kayserili H, Kimonis V, Wu E, Mellado C, Aggarwal V, Richieri-Costa A, Brunoni D, Canó TM, Jorge AAL, Kim CA, Honjo R, Bertola DR, Dandalo-Girardi RM, Bayram Y, Gezdirici A, Yilmaz-Gulec E, Gumus E, Yilmaz GC, Okamoto N, Ohashi H, Coban–Akdemir Z, Mitani T, Jhangiani SN, Muzny DM, Regattieri NAP, Pogue R, Pereira RW, Otto PA, Gibbs RA, Ali BR, van Bokhoven H, Brunner HG, Sutton VR, Lupski JR, Vianna-Morgante AM, Carvalho CMB, Mazzeu JF. Phenotypic and mutational spectrum of ROR2-related Robinow syndrome [Internet]. Human Mutation. 2022 ; 43( 7): 900-918.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1002/humu.24375
Artigo de periodico
Diagnostic yield of a multigene sequencing approach in children classified as idiopathic short stature (2022)
Andrade, Nathalia Liberatoscioli Menezes; Funari, Mariana Ferreira de Assis; Scalco, Renata; Dantas, Naiara Castelo Branc; Rezende, Raissa C; Freire, Bruna L; Krepischi, Ana Cristina Victorino ; Arnhold, Ivo J P; Jorge, Alexander A. L; Vasques, Gabriela Andrade
Source: Endocrine Connections. Unidades: IB, FM
Subjects: MUTAÇÃO GENÉTICA, SEQUENCIAMENTO GENÉTICO, CRIANÇAS, DOENÇAS GENÉTICAS
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ABNT
ANDRADE, Nathalia Liberatoscioli Menezes et al. Diagnostic yield of a multigene sequencing approach in children classified as idiopathic short stature. Endocrine Connections, v. 11, n. 12, 2022Tradução . . Disponível em: https://doi.org/10.1530/EC-22-0214. Acesso em: 03 jul. 2024.
APA
Andrade, N. L. M., Funari, M. F. de A., Scalco, R., Dantas, N. C. B., Rezende, R. C., Freire, B. L., et al. (2022). Diagnostic yield of a multigene sequencing approach in children classified as idiopathic short stature. Endocrine Connections, 11( 12). doi:10.1530/EC-22-0214
NLM
Andrade NLM, Funari MF de A, Scalco R, Dantas NCB, Rezende RC, Freire BL, Krepischi ACV, Arnhold IJP, Jorge AAL, Vasques GA. Diagnostic yield of a multigene sequencing approach in children classified as idiopathic short stature [Internet]. Endocrine Connections. 2022 ; 11( 12):[citado 2024 jul. 03 ] Available from: https://doi.org/10.1530/EC-22-0214
Vancouver
Andrade NLM, Funari MF de A, Scalco R, Dantas NCB, Rezende RC, Freire BL, Krepischi ACV, Arnhold IJP, Jorge AAL, Vasques GA. Diagnostic yield of a multigene sequencing approach in children classified as idiopathic short stature [Internet]. Endocrine Connections. 2022 ; 11( 12):[citado 2024 jul. 03 ] Available from: https://doi.org/10.1530/EC-22-0214
Artigo de periodico
Evaluation of SHOX defects in the era of next-generation sequencing (2019)
Funari, Mariana F. A; Barros, Juliana S. de; Santana, Lucas S; Lerario, Antonio M; Freire, Bruna L; Homma, Thais K; Vasques, Gabriela A; Mendonça, Berenice Bilharinho de ; Nishi, Mirian Y; Jorge, Alexander Augusto de Lima
Source: Clinical genetics. Unidade: FM
Subjects: GENES HOMEOBOX, MUTAÇÃO, INSUFICIÊNCIA DE CRESCIMENTO, GENÔMICA, SEQUENCIAMENTO GENÉTICO
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ABNT
FUNARI, Mariana F. A et al. Evaluation of SHOX defects in the era of next-generation sequencing. Clinical genetics, v. 96, n. 3, p. 261-265, 2019Tradução . . Disponível em: https://doi.org/10.1111/cge.13587. Acesso em: 03 jul. 2024.
APA
Funari, M. F. A., Barros, J. S. de, Santana, L. S., Lerario, A. M., Freire, B. L., Homma, T. K., et al. (2019). Evaluation of SHOX defects in the era of next-generation sequencing. Clinical genetics, 96( 3), 261-265. doi:10.1111/cge.13587
NLM
Funari MFA, Barros JS de, Santana LS, Lerario AM, Freire BL, Homma TK, Vasques GA, Mendonça BB de, Nishi MY, Jorge AA de L. Evaluation of SHOX defects in the era of next-generation sequencing [Internet]. Clinical genetics. 2019 ; 96( 3): 261-265.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1111/cge.13587
Vancouver
Funari MFA, Barros JS de, Santana LS, Lerario AM, Freire BL, Homma TK, Vasques GA, Mendonça BB de, Nishi MY, Jorge AA de L. Evaluation of SHOX defects in the era of next-generation sequencing [Internet]. Clinical genetics. 2019 ; 96( 3): 261-265.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1111/cge.13587
Artigo de periodico
Genetic diagnosis of congenital hypopituitarism by a target gene panel: novel pathogenic variants in GLI2, OTX2 and GHRHR (2019)
Nakaguma, Marilena; Correa, Fernanda A; Santana, Lucas S; Benedetti, Anna F. F; V, Ricardo Perez; Huayllas, Martha K. P; Miras, Mirta B; Funari, Mariana F. A; Lerario, Antonio M; Mendonça, Berenice Bilharinho de; Jorge, Alexander Augusto de Lima
Source: Endocrine connections. Unidade: FM
Subjects: HORMÔNIOS DA ADENO-HIPÓFISE, DOENÇAS CONGÊNITAS, SEQUENCIAMENTO GENÉTICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NAKAGUMA, Marilena et al. Genetic diagnosis of congenital hypopituitarism by a target gene panel: novel pathogenic variants in GLI2, OTX2 and GHRHR. Endocrine connections, v. 8, n. 5, p. 590-595, 2019Tradução . . Disponível em: https://doi.org/10.1530/EC-19-0085. Acesso em: 03 jul. 2024.
APA
Nakaguma, M., Correa, F. A., Santana, L. S., Benedetti, A. F. F., V, R. P., Huayllas, M. K. P., et al. (2019). Genetic diagnosis of congenital hypopituitarism by a target gene panel: novel pathogenic variants in GLI2, OTX2 and GHRHR. Endocrine connections, 8( 5), 590-595. doi:10.1530/EC-19-0085
NLM
Nakaguma M, Correa FA, Santana LS, Benedetti AFF, V RP, Huayllas MKP, Miras MB, Funari MFA, Lerario AM, Mendonça BB de, Jorge AA de L. Genetic diagnosis of congenital hypopituitarism by a target gene panel: novel pathogenic variants in GLI2, OTX2 and GHRHR [Internet]. Endocrine connections. 2019 ; 8( 5): 590-595.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1530/EC-19-0085
Vancouver
Nakaguma M, Correa FA, Santana LS, Benedetti AFF, V RP, Huayllas MKP, Miras MB, Funari MFA, Lerario AM, Mendonça BB de, Jorge AA de L. Genetic diagnosis of congenital hypopituitarism by a target gene panel: novel pathogenic variants in GLI2, OTX2 and GHRHR [Internet]. Endocrine connections. 2019 ; 8( 5): 590-595.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1530/EC-19-0085
Artigo de periodico
Genetic Disorders in Prenatal Onset Syndromic Short Stature Identified by Exome Sequencing (2019)
Homma, Thais Kataoka; Freire, Bruna Lucheze; Kawahira, Rachel Sayuri Honjo; Dauber, Andrew; Funari, Mariana Ferreira de Assis; Lerario, Antonio Marcondes; Nishi, Mirian Yumie; Albuquerque, Edoarda Vasco de; Kim, Chong Ae ; Jorge, Alexander Augusto de Lima
Source: Journal of pediatrics. Unidade: FM
Subjects: TRANSTORNOS DO CRESCIMENTO, RECÉM-NASCIDO PEQUENO PARA IDADE GESTACIONAL, SEQUENCIAMENTO GENÉTICO, ESTATURA, RECÉM-NASCIDO, LACTENTES
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ABNT
HOMMA, Thais Kataoka et al. Genetic Disorders in Prenatal Onset Syndromic Short Stature Identified by Exome Sequencing. Journal of pediatrics, v. 215, p. 192-198, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.jpeds.2019.08.024. Acesso em: 03 jul. 2024.
APA
Homma, T. K., Freire, B. L., Kawahira, R. S. H., Dauber, A., Funari, M. F. de A., Lerario, A. M., et al. (2019). Genetic Disorders in Prenatal Onset Syndromic Short Stature Identified by Exome Sequencing. Journal of pediatrics, 215, 192-198. doi:10.1016/j.jpeds.2019.08.024
NLM
Homma TK, Freire BL, Kawahira RSH, Dauber A, Funari MF de A, Lerario AM, Nishi MY, Albuquerque EV de, Kim CA, Jorge AA de L. Genetic Disorders in Prenatal Onset Syndromic Short Stature Identified by Exome Sequencing [Internet]. Journal of pediatrics. 2019 ; 215 192-198.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1016/j.jpeds.2019.08.024
Vancouver
Homma TK, Freire BL, Kawahira RSH, Dauber A, Funari MF de A, Lerario AM, Nishi MY, Albuquerque EV de, Kim CA, Jorge AA de L. Genetic Disorders in Prenatal Onset Syndromic Short Stature Identified by Exome Sequencing [Internet]. Journal of pediatrics. 2019 ; 215 192-198.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1016/j.jpeds.2019.08.024
Artigo de periodico
Germline mutation landscape of multiple endocrine neoplasia type 1 using full gene next-generation sequencing (2018)
Carvalho, Rafael A.; Jorge, Alexander Augusto de Lima; Toledo, Sergio Pereira de Almeida
Source: European journal of endocrinology. Unidade: FM
Subjects: NEOPLASIAS DAS PARATIREOIDES, MUTAÇÃO GENÉTICA, SEQUENCIAMENTO GENÉTICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CARVALHO, Rafael A. e JORGE, Alexander Augusto de Lima e TOLEDO, Sergio Pereira de Almeida. Germline mutation landscape of multiple endocrine neoplasia type 1 using full gene next-generation sequencing. European journal of endocrinology, v. 179, n. 6, p. 391-407, 2018Tradução . . Disponível em: https://doi.org/10.1530/EJE-18-0430. Acesso em: 03 jul. 2024.
APA
Carvalho, R. A., Jorge, A. A. de L., & Toledo, S. P. de A. (2018). Germline mutation landscape of multiple endocrine neoplasia type 1 using full gene next-generation sequencing. European journal of endocrinology, 179( 6), 391-407. doi:10.1530/EJE-18-0430
NLM
Carvalho RA, Jorge AA de L, Toledo SP de A. Germline mutation landscape of multiple endocrine neoplasia type 1 using full gene next-generation sequencing [Internet]. European journal of endocrinology. 2018 ; 179( 6): 391-407.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1530/EJE-18-0430
Vancouver
Carvalho RA, Jorge AA de L, Toledo SP de A. Germline mutation landscape of multiple endocrine neoplasia type 1 using full gene next-generation sequencing [Internet]. European journal of endocrinology. 2018 ; 179( 6): 391-407.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1530/EJE-18-0430
Trabalho de evento-resumo periodico
Molecular analysis of brazilian patients with combined pituitary hormone deficiency (CPHD) and orthotopic posterior pituitary lobe (OPP) reveals 8 different PROP1 alterations with three novel mutations (2017)
Madeira, Joao L. O.; Jorge, Alexander Augusto de Lima; Mendonça, Berenice Bilharinho de
Source: Hormone research in paediatrics. Conference titles: Joint meeting of paediatric endocrinology. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, HORMÔNIOS HIPOFISÁRIOS, SEQUENCIAMENTO GENÉTICO, ESTUDOS DE COORTES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MADEIRA, Joao L. O. e JORGE, Alexander Augusto de Lima e MENDONÇA, Berenice Bilharinho de. Molecular analysis of brazilian patients with combined pituitary hormone deficiency (CPHD) and orthotopic posterior pituitary lobe (OPP) reveals 8 different PROP1 alterations with three novel mutations. Hormone research in paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 03 jul. 2024. , 2017
APA
Madeira, J. L. O., Jorge, A. A. de L., & Mendonça, B. B. de. (2017). Molecular analysis of brazilian patients with combined pituitary hormone deficiency (CPHD) and orthotopic posterior pituitary lobe (OPP) reveals 8 different PROP1 alterations with three novel mutations. Hormone research in paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo.
NLM
Madeira JLO, Jorge AA de L, Mendonça BB de. Molecular analysis of brazilian patients with combined pituitary hormone deficiency (CPHD) and orthotopic posterior pituitary lobe (OPP) reveals 8 different PROP1 alterations with three novel mutations. Hormone research in paediatrics. 2017 ; 88 43-44.[citado 2024 jul. 03 ]
Vancouver
Madeira JLO, Jorge AA de L, Mendonça BB de. Molecular analysis of brazilian patients with combined pituitary hormone deficiency (CPHD) and orthotopic posterior pituitary lobe (OPP) reveals 8 different PROP1 alterations with three novel mutations. Hormone research in paediatrics. 2017 ; 88 43-44.[citado 2024 jul. 03 ]
Artigo de periodico
Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations with three novel mutations (2017)
Madeira, Joao Lo; Jorge, Alexander Augusto de Lima; Mendonça, Berenice Bilharinho de
Source: Clinical endocrinology. Unidade: FM
Subjects: HORMÔNIOS HIPOFISÁRIOS, SEQUENCIAMENTO GENÉTICO, BRASILEIROS, ESTUDOS DE COORTES, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MADEIRA, Joao Lo e JORGE, Alexander Augusto de Lima e MENDONÇA, Berenice Bilharinho de. Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations with three novel mutations. Clinical endocrinology, v. 87, n. 6, p. 725-732, 2017Tradução . . Disponível em: https://doi.org/10.1111/cen.13430. Acesso em: 03 jul. 2024.
APA
Madeira, J. L., Jorge, A. A. de L., & Mendonça, B. B. de. (2017). Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations with three novel mutations. Clinical endocrinology, 87( 6), 725-732. doi:10.1111/cen.13430
NLM
Madeira JL, Jorge AA de L, Mendonça BB de. Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations with three novel mutations [Internet]. Clinical endocrinology. 2017 ; 87( 6): 725-732.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1111/cen.13430
Vancouver
Madeira JL, Jorge AA de L, Mendonça BB de. Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations with three novel mutations [Internet]. Clinical endocrinology. 2017 ; 87( 6): 725-732.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1111/cen.13430
Artigo de periodico
Whole Exome Sequencing in the Investigation of Growth Disorders, Including Patients with Primary IGF-1 Deficiency (2017)
Jorge, Alexander Augusto de Lima
Source: Hormone research in paediatrics. Unidade: FM
Subjects: ESTATURA, SEQUENCIAMENTO GENÉTICO, TRANSTORNOS DO CRESCIMENTO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
JORGE, Alexander Augusto de Lima. Whole Exome Sequencing in the Investigation of Growth Disorders, Including Patients with Primary IGF-1 Deficiency. Hormone research in paediatrics, v. 88, n. 6, p. 421-422, 2017Tradução . . Disponível em: https://doi.org/10.1159/000481792. Acesso em: 03 jul. 2024.
APA
Jorge, A. A. de L. (2017). Whole Exome Sequencing in the Investigation of Growth Disorders, Including Patients with Primary IGF-1 Deficiency. Hormone research in paediatrics, 88( 6), 421-422. doi:10.1159/000481792
NLM
Jorge AA de L. Whole Exome Sequencing in the Investigation of Growth Disorders, Including Patients with Primary IGF-1 Deficiency [Internet]. Hormone research in paediatrics. 2017 ; 88( 6): 421-422.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1159/000481792
Vancouver
Jorge AA de L. Whole Exome Sequencing in the Investigation of Growth Disorders, Including Patients with Primary IGF-1 Deficiency [Internet]. Hormone research in paediatrics. 2017 ; 88( 6): 421-422.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1159/000481792
Artigo de periodico
Further evidence of the importance of RIT1 in Noonan syndrome (2014)
Bertola, Débora Romeo; Yamamoto, Guilherme L; Almeida, Tatiana F; Buscarilli, Michele; Jorge, Alexander A L; Malaquias, Alexsandra C; Kim, Chong A; Takahashi, Vanessa N. V; Passos-Bueno, Maria Rita ; Pereira, Alexandre C
Source: American Journal of Medical Genetics Part A. Unidades: IB, FM
Subjects: FENÓTIPOS, HIPERTROFIA VENTRICULAR ESQUERDA, MUTAÇÃO GENÉTICA, SEQUENCIAMENTO GENÉTICO, ANORMALIDADES CARDIOVASCULARES, INSUFICIÊNCIA DE CRESCIMENTO
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ABNT
BERTOLA, Débora Romeo et al. Further evidence of the importance of RIT1 in Noonan syndrome. American Journal of Medical Genetics Part A, p. 1-6, 2014Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.36722. Acesso em: 03 jul. 2024.
APA
Bertola, D. R., Yamamoto, G. L., Almeida, T. F., Buscarilli, M., Jorge, A. A. L., Malaquias, A. C., et al. (2014). Further evidence of the importance of RIT1 in Noonan syndrome. American Journal of Medical Genetics Part A, 1-6. doi:10.1002/ajmg.a.36722
NLM
Bertola DR, Yamamoto GL, Almeida TF, Buscarilli M, Jorge AAL, Malaquias AC, Kim CA, Takahashi VNV, Passos-Bueno MR, Pereira AC. Further evidence of the importance of RIT1 in Noonan syndrome [Internet]. American Journal of Medical Genetics Part A. 2014 ; 1-6.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1002/ajmg.a.36722
Vancouver
Bertola DR, Yamamoto GL, Almeida TF, Buscarilli M, Jorge AAL, Malaquias AC, Kim CA, Takahashi VNV, Passos-Bueno MR, Pereira AC. Further evidence of the importance of RIT1 in Noonan syndrome [Internet]. American Journal of Medical Genetics Part A. 2014 ; 1-6.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1002/ajmg.a.36722
Trabalho de evento-resumo periodico
Novel mutations (P.G6R and P.R511W) in IGF1R gene in children born small for gestational age (SGA) without catch-up growth (2010)
Leal, A C; Montenegro, Luciana Ribeiro; Coutinho, D C; Mendonça, Berenice Bilharinho de; Arnhold, I J P; Jorge, Alexander Augusto de Lima
Source: Clinics. Conference titles: Simpósio "Avanços em Pesquisas Médicas dos Laboratórios de Investigação Médica do Hospital das Clínicas da FMUSP". Unidade: FM
Subjects: RECÉM-NASCIDO PEQUENO PARA IDADE GESTACIONAL, MUTAÇÃO GENÉTICA, TRANSTORNOS DO CRESCIMENTO (GENÉTICA), SEQUENCIAMENTO GENÉTICO, RESUMOS (EVENTOS)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LEAL, A C et al. Novel mutations (P.G6R and P.R511W) in IGF1R gene in children born small for gestational age (SGA) without catch-up growth. Clinics. São Paulo: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 03 jul. 2024. , 2010
APA
Leal, A. C., Montenegro, L. R., Coutinho, D. C., Mendonça, B. B. de, Arnhold, I. J. P., & Jorge, A. A. de L. (2010). Novel mutations (P.G6R and P.R511W) in IGF1R gene in children born small for gestational age (SGA) without catch-up growth. Clinics. São Paulo: Faculdade de Medicina, Universidade de São Paulo.
NLM
Leal AC, Montenegro LR, Coutinho DC, Mendonça BB de, Arnhold IJP, Jorge AA de L. Novel mutations (P.G6R and P.R511W) in IGF1R gene in children born small for gestational age (SGA) without catch-up growth. Clinics. 2010 ; 65 S64.[citado 2024 jul. 03 ]
Vancouver
Leal AC, Montenegro LR, Coutinho DC, Mendonça BB de, Arnhold IJP, Jorge AA de L. Novel mutations (P.G6R and P.R511W) in IGF1R gene in children born small for gestational age (SGA) without catch-up growth. Clinics. 2010 ; 65 S64.[citado 2024 jul. 03 ]

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