Varela, M. C.; Kok, Fernando; Setian, Nuvarte; Kim, C. A.; Koiffmann, Celia Priszkulnik 
Source: Clinical Genetics. Unidades: FM, IB
Subjects: PSICOMOTRICIDADE, MUTAÇÃO GENÉTICA, RETARDO MENTAL
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VARELA, M. C. et al. Impact of molecular mechanisms, including deletion size, on Prader-Willi syndrome phenotype: study of 75 patients. Clinical Genetics, v. 67, n. 1, p. 47-52, 2005Tradução . . Disponível em: https://doi.org/10.1111/j.1399-0004.2005.00377.x. Acesso em: 15 nov. 2024.APA
Varela, M. C., Kok, F., Setian, N., Kim, C. A., & Koiffmann, C. P. (2005). Impact of molecular mechanisms, including deletion size, on Prader-Willi syndrome phenotype: study of 75 patients. Clinical Genetics, 67( 1), 47-52. doi:10.1111/j.1399-0004.2005.00377.xNLM
Varela MC, Kok F, Setian N, Kim CA, Koiffmann CP. Impact of molecular mechanisms, including deletion size, on Prader-Willi syndrome phenotype: study of 75 patients [Internet]. Clinical Genetics. 2005 ; 67( 1): 47-52.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1111/j.1399-0004.2005.00377.xVancouver
Varela MC, Kok F, Setian N, Kim CA, Koiffmann CP. Impact of molecular mechanisms, including deletion size, on Prader-Willi syndrome phenotype: study of 75 patients [Internet]. Clinical Genetics. 2005 ; 67( 1): 47-52.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1111/j.1399-0004.2005.00377.x
