Varela, C.; Kok, Fernando; Setian, Nuvarte; Kim, C A; Koiffmann, Celia Priszkulnik 
Source: Abstracts. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidades: FM, IB
Subjects: MUTAÇÃO GENÉTICA, DOENÇAS GENÉTICAS
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VARELA, C. et al. Is the Prader-Willi syndrome phenotype related to molecular mechanisms? A study of 75 patients. 2004, Anais.. Toronto: Faculdade de Medicina, Universidade de São Paulo, 2004. . Acesso em: 18 nov. 2024.APA
Varela, C., Kok, F., Setian, N., Kim, C. A., & Koiffmann, C. P. (2004). Is the Prader-Willi syndrome phenotype related to molecular mechanisms? A study of 75 patients. In Abstracts. Toronto: Faculdade de Medicina, Universidade de São Paulo.NLM
Varela C, Kok F, Setian N, Kim CA, Koiffmann CP. Is the Prader-Willi syndrome phenotype related to molecular mechanisms? A study of 75 patients. Abstracts. 2004 ;[citado 2024 nov. 18 ]Vancouver
Varela C, Kok F, Setian N, Kim CA, Koiffmann CP. Is the Prader-Willi syndrome phenotype related to molecular mechanisms? A study of 75 patients. Abstracts. 2004 ;[citado 2024 nov. 18 ]
