Impact of molecular mechanisms, including deletion size, on Prader-Willi syndrome phenotype: study of 75 patients (2005)
- Authors:
- USP affiliated authors: SETIAN, NUVARTE - FM ; KOIFFMANN, CELIA PRISZKULNIK - IB
- Unidades: FM; IB
- DOI: 10.1111/j.1399-0004.2005.00377.x
- Subjects: PSICOMOTRICIDADE; MUTAÇÃO GENÉTICA; RETARDO MENTAL
- Language: Inglês
- Imprenta:
- Publisher place: Copenhagen
- Date published: 2005
- Source:
- Título: Clinical Genetics
- ISSN: 1399-0004
- Volume/Número/Paginação/Ano: v. 67, n. 1, p. 47-52, 2005
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
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: 28 dez. 2025. -
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.x -
NLM
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 2025 dez. 28 ] Available from: https://doi.org/10.1111/j.1399-0004.2005.00377.x -
Vancouver
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 2025 dez. 28 ] Available from: https://doi.org/10.1111/j.1399-0004.2005.00377.x - Is the Prader-Willi syndrome phenotype related to molecular mechanisms? A study of 75 patients
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Informações sobre o DOI: 10.1111/j.1399-0004.2005.00377.x (Fonte: oaDOI API)
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