Prader-Willi syndrome: genetic tests and clinical findings (2000)
- Authors:
- USP affiliated authors: KOIFFMANN, CELIA PRISZKULNIK - IB ; SETIAN, NUVARTE - FM
- Unidades: IB; FM
- Subjects: GENÉTICA MÉDICA; MALFORMAÇÕES; FENÓTIPOS (ASPECTOS MÉDICOS)
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Genetic Testing
- ISSN: 1090-6576
- Volume/Número/Paginação/Ano: v. 4, n. 4, p. 387-392, 2000
-
ABNT
FRIDMAN, Cintia et al. Prader-Willi syndrome: genetic tests and clinical findings. Genetic Testing, v. 4, n. 4, p. 387-392, 2000Tradução . . Acesso em: 22 jul. 2024. -
APA
Fridman, C., Varela, M. C., Kok, F., Setian, N., & Koiffmann, C. P. (2000). Prader-Willi syndrome: genetic tests and clinical findings. Genetic Testing, 4( 4), 387-392. -
NLM
Fridman C, Varela MC, Kok F, Setian N, Koiffmann CP. Prader-Willi syndrome: genetic tests and clinical findings. Genetic Testing. 2000 ; 4( 4): 387-392.[citado 2024 jul. 22 ] -
Vancouver
Fridman C, Varela MC, Kok F, Setian N, Koiffmann CP. Prader-Willi syndrome: genetic tests and clinical findings. Genetic Testing. 2000 ; 4( 4): 387-392.[citado 2024 jul. 22 ] - Is the Prader-Willi syndrome phenotype related to molecular mechanisms? A study of 75 patients
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