Source: European Journal of Medical Genetics. Unidade: IB
Subjects: ANORMALIDADES CROMOSSÔMICAS, OBESIDADE
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: 30 set. 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.2006.02.001NLM
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 set. 30 ] Available from: https://doi.org/10.1016/j.ejmg.2006.02.001Vancouver
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 set. 30 ] Available from: https://doi.org/10.1016/j.ejmg.2006.02.001