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Filtros : "Castro, Cláudia Irene Emílio de" "2006" Limpar

Filtros

Artigo de periodico
A new case of interstitial 6q16.2 deletion in a patient with Prader-Willi-like phenotype and investigation of SIM1 gene deletion in 87 patients with syndromic obesity (2006)
Varela, Monica Castro; Simões-Sato, Alex Y.; Kim, Chong A.; Bertola, Débora Romeo; Castro, Cláudia Irene Emílio de; Koiffmann, Celia Priszkulnik
Source: European Journal of Medical Genetics. Unidade: IB
Subjects: ANORMALIDADES CROMOSSÔMICAS, OBESIDADE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VARELA, Monica Castro et al. A new case of interstitial 6q16.2 deletion in a patient with Prader-Willi-like phenotype and investigation of SIM1 gene deletion in 87 patients with syndromic obesity. European Journal of Medical Genetics, v. 49, n. 4, p. 298-305, 2006Tradução . . Acesso em: 01 nov. 2024.
APA
Varela, M. C., Simões-Sato, A. Y., Kim, C. A., Bertola, D. R., Castro, C. I. E. de, & Koiffmann, C. P. (2006). A new case of interstitial 6q16.2 deletion in a patient with Prader-Willi-like phenotype and investigation of SIM1 gene deletion in 87 patients with syndromic obesity. European Journal of Medical Genetics, 49( 4), 298-305.
NLM
Varela MC, Simões-Sato AY, Kim CA, Bertola DR, Castro CIE de, Koiffmann CP. A new case of interstitial 6q16.2 deletion in a patient with Prader-Willi-like phenotype and investigation of SIM1 gene deletion in 87 patients with syndromic obesity. European Journal of Medical Genetics. 2006 ; 49( 4): 298-305.[citado 2024 nov. 01 ]
Vancouver
Varela MC, Simões-Sato AY, Kim CA, Bertola DR, Castro CIE de, Koiffmann CP. A new case of interstitial 6q16.2 deletion in a patient with Prader-Willi-like phenotype and investigation of SIM1 gene deletion in 87 patients with syndromic obesity. European Journal of Medical Genetics. 2006 ; 49( 4): 298-305.[citado 2024 nov. 01 ]
Artigo de periodico
Prader-Willi-like phenotype: investigation of 1p36 deletion in 41 patients with delayed psychomotor development, hypotonia, obesity and/or hyperphagia, learning disabilities and behavioral problems (2006)
D'Angelo, Carla Sustek; Paz, José A. da; Kim, Chong A.; Bertola, Débora Romeo; Castro, Cláudia Irene Emílio de; Varela, Monica Castro; Koiffmann, Celia Priszkulnik
Source: European Journal of Medical Genetics. Unidade: IB
Subjects: ANORMALIDADES CROMOSSÔMICAS, OBESIDADE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
D'ANGELO, Carla Sustek et al. Prader-Willi-like phenotype: investigation of 1p36 deletion in 41 patients with delayed psychomotor development, hypotonia, obesity and/or hyperphagia, learning disabilities and behavioral problems. European Journal of Medical Genetics, v. 49, n. 6, p. 451-460, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.ejmg.2006.02.001. Acesso em: 01 nov. 2024.
APA
D'Angelo, C. S., Paz, J. A. da, Kim, C. A., Bertola, D. R., Castro, C. I. E. de, Varela, M. C., & Koiffmann, C. P. (2006). Prader-Willi-like phenotype: investigation of 1p36 deletion in 41 patients with delayed psychomotor development, hypotonia, obesity and/or hyperphagia, learning disabilities and behavioral problems. European Journal of Medical Genetics, 49( 6), 451-460. doi:10.1016/j.ejmg.2006.02.001
NLM
D'Angelo CS, Paz JA da, Kim CA, Bertola DR, Castro CIE de, Varela MC, Koiffmann CP. Prader-Willi-like phenotype: investigation of 1p36 deletion in 41 patients with delayed psychomotor development, hypotonia, obesity and/or hyperphagia, learning disabilities and behavioral problems [Internet]. European Journal of Medical Genetics. 2006 ; 49( 6): 451-460.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.ejmg.2006.02.001
Vancouver
D'Angelo CS, Paz JA da, Kim CA, Bertola DR, Castro CIE de, Varela MC, Koiffmann CP. Prader-Willi-like phenotype: investigation of 1p36 deletion in 41 patients with delayed psychomotor development, hypotonia, obesity and/or hyperphagia, learning disabilities and behavioral problems [Internet]. European Journal of Medical Genetics. 2006 ; 49( 6): 451-460.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.ejmg.2006.02.001

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