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Trabalho de evento-resumo periodico
Analysis of major causative hypogonadotropic hypogonadism genes in patients with constitutional delay of growth and puberty (2012)
Silveira, Leticia F. G.; Tusset, Cintia; Moura, Lucas; Beneduzzi, Daiane; Teles, Milena; Jorge, Alexander A. L.; Trarbach, Ericka B.; Latronico, Ana Claudia
Source: Hormone research in paediatrics. Conference titles: 51th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE). Unidade: FM
Subjects: HIPOGONADISMO (DIAGNÓSTICO), GENES, CRESCIMENTO (DEFICIÊNCIA), FENÓTIPOS, POLIMORFISMO, DOENÇAS GENÉTICAS (DIAGNÓSTICO), RESUMOS (EVENTOS)
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ABNT
SILVEIRA, Leticia F. G. et al. Analysis of major causative hypogonadotropic hypogonadism genes in patients with constitutional delay of growth and puberty. Hormone research in paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1159/000343182. Acesso em: 16 nov. 2024. , 2012
APA
Silveira, L. F. G., Tusset, C., Moura, L., Beneduzzi, D., Teles, M., Jorge, A. A. L., et al. (2012). Analysis of major causative hypogonadotropic hypogonadism genes in patients with constitutional delay of growth and puberty. Hormone research in paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. doi:10.1159/000343182
NLM
Silveira LFG, Tusset C, Moura L, Beneduzzi D, Teles M, Jorge AAL, Trarbach EB, Latronico AC. Analysis of major causative hypogonadotropic hypogonadism genes in patients with constitutional delay of growth and puberty [Internet]. Hormone research in paediatrics. 2012 ;78( suppl. 1): 119.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1159/000343182
Vancouver
Silveira LFG, Tusset C, Moura L, Beneduzzi D, Teles M, Jorge AAL, Trarbach EB, Latronico AC. Analysis of major causative hypogonadotropic hypogonadism genes in patients with constitutional delay of growth and puberty [Internet]. Hormone research in paediatrics. 2012 ;78( suppl. 1): 119.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1159/000343182
Trabalho de evento-resumo periodico
Contiguous Gene Syndrome Caused by an Interstitial Deletion in the Short Arm of X-chromosome Diagnosed by MLPA (2010)
Alves, B. B.; Silveira, L. F. G.; Teles, M.; Nishi, M. Y.; Funari, M. F. A.; Mendonça, B. B.
Source: Hormone Research in Paediatrics. Conference titles: Annual meeting of the Sociedad Latino-Americana de Endocrinología Pediátrica (SLEP). Unidade: FM
Subjects: DELEÇÃO DE GENES, DOENÇAS GENÉTICAS (DIAGNÓSTICO), CROMOSSOMO X (PATOLOGIA), FENÓTIPOS (ANORMALIDADES)
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ABNT
ALVES, B. B. et al. Contiguous Gene Syndrome Caused by an Interstitial Deletion in the Short Arm of X-chromosome Diagnosed by MLPA. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Disponível em: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=320138&Ausgabe=254526&ProduktNr=224036&filename=320138.pdf. Acesso em: 16 nov. 2024. , 2010
APA
Alves, B. B., Silveira, L. F. G., Teles, M., Nishi, M. Y., Funari, M. F. A., & Mendonça, B. B. (2010). Contiguous Gene Syndrome Caused by an Interstitial Deletion in the Short Arm of X-chromosome Diagnosed by MLPA. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Recuperado de http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=320138&Ausgabe=254526&ProduktNr=224036&filename=320138.pdf
NLM
Alves BB, Silveira LFG, Teles M, Nishi MY, Funari MFA, Mendonça BB. Contiguous Gene Syndrome Caused by an Interstitial Deletion in the Short Arm of X-chromosome Diagnosed by MLPA [Internet]. Hormone Research in Paediatrics. 2010 ; 74( suppl. 1): 21.[citado 2024 nov. 16 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=320138&Ausgabe=254526&ProduktNr=224036&filename=320138.pdf
Vancouver
Alves BB, Silveira LFG, Teles M, Nishi MY, Funari MFA, Mendonça BB. Contiguous Gene Syndrome Caused by an Interstitial Deletion in the Short Arm of X-chromosome Diagnosed by MLPA [Internet]. Hormone Research in Paediatrics. 2010 ; 74( suppl. 1): 21.[citado 2024 nov. 16 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=320138&Ausgabe=254526&ProduktNr=224036&filename=320138.pdf
Artigo de periodico
Report of a del22q11 in a patient with Mayer-Rokitansky-Kuster-Hauser (MRKH) anomaly and exclusion of WNT-4, RAR-gamma, and RXR-alpha as major genes determining MRKH anomaly in a study of 25 affected women (2006)
Cheroki, Carola; Krepischi, Ana Cristina Victorino ; Rosenberg, Carla ; Jehee, Fernanda Sarquis; Mingroni Netto, Regina Celia ; Pavanello Filho, Ivo; Zanforlin Filho, Sabastião; Kim, Chong Ae; Bagnoli, Vicente Renato; Mendonça, Berenice B.; Szuhai, Karoly; Otto, Paulo A
Source: American Journal of Medical Genetics. Part A. Unidades: IB, FM
Subjects: DOENÇAS GENÉTICAS (DIAGNÓSTICO), GENES (ANÁLISE), ANOMALIA FACIAL (GENÉTICA), POLIMORFISMO (GENÉTICA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CHEROKI, Carola et al. Report of a del22q11 in a patient with Mayer-Rokitansky-Kuster-Hauser (MRKH) anomaly and exclusion of WNT-4, RAR-gamma, and RXR-alpha as major genes determining MRKH anomaly in a study of 25 affected women. American Journal of Medical Genetics. Part A, v. 140A, n. 12, p. 1339-1342, 2006Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.31254. Acesso em: 16 nov. 2024.
APA
Cheroki, C., Krepischi, A. C. V., Rosenberg, C., Jehee, F. S., Mingroni Netto, R. C., Pavanello Filho, I., et al. (2006). Report of a del22q11 in a patient with Mayer-Rokitansky-Kuster-Hauser (MRKH) anomaly and exclusion of WNT-4, RAR-gamma, and RXR-alpha as major genes determining MRKH anomaly in a study of 25 affected women. American Journal of Medical Genetics. Part A, 140A( 12), 1339-1342. doi:10.1002/ajmg.a.31254
NLM
Cheroki C, Krepischi ACV, Rosenberg C, Jehee FS, Mingroni Netto RC, Pavanello Filho I, Zanforlin Filho S, Kim CA, Bagnoli VR, Mendonça BB, Szuhai K, Otto PA. Report of a del22q11 in a patient with Mayer-Rokitansky-Kuster-Hauser (MRKH) anomaly and exclusion of WNT-4, RAR-gamma, and RXR-alpha as major genes determining MRKH anomaly in a study of 25 affected women [Internet]. American Journal of Medical Genetics. Part A. 2006 ; 140A( 12): 1339-1342.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/ajmg.a.31254
Vancouver
Cheroki C, Krepischi ACV, Rosenberg C, Jehee FS, Mingroni Netto RC, Pavanello Filho I, Zanforlin Filho S, Kim CA, Bagnoli VR, Mendonça BB, Szuhai K, Otto PA. Report of a del22q11 in a patient with Mayer-Rokitansky-Kuster-Hauser (MRKH) anomaly and exclusion of WNT-4, RAR-gamma, and RXR-alpha as major genes determining MRKH anomaly in a study of 25 affected women [Internet]. American Journal of Medical Genetics. Part A. 2006 ; 140A( 12): 1339-1342.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/ajmg.a.31254

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