A new case of interstitial 6q16.2 deletion in a patient with Prader-Willi-Like phenotype and investigation of SIM1 gene deletion in 87 patients with sindromic obesity (2005)
- Authors:
- Autor USP: KOIFFMANN, CELIA PRISZKULNIK - IB
- Unidade: IB
- Subjects: OBESIDADE; ANORMALIDADES CROMOSSÔMICAS
- Language: Inglês
- Imprenta:
- Publisher place: Salt Lake City
- Date published: 2005
- Source:
- Título: Abstracts
- Conference titles: Annual Meeting of the American Society of Human Genetics
-
ABNT
VARELA, M. C. et al. A new case of interstitial 6q16.2 deletion in a patient with Prader-Willi-Like phenotype and investigation of SIM1 gene deletion in 87 patients with sindromic obesity. 2005, Anais.. Salt Lake City: Instituto de Biociências, Universidade de São Paulo, 2005. . Acesso em: 10 jan. 2026. -
APA
Varela, M. C., Kim, C. A., Bertola, D. R., Simões-Sato, A. Y., Castro, C. I. E., & Koiffmann, C. P. (2005). A new case of interstitial 6q16.2 deletion in a patient with Prader-Willi-Like phenotype and investigation of SIM1 gene deletion in 87 patients with sindromic obesity. In Abstracts. Salt Lake City: Instituto de Biociências, Universidade de São Paulo. -
NLM
Varela MC, Kim CA, Bertola DR, Simões-Sato AY, Castro CIE, Koiffmann CP. A new case of interstitial 6q16.2 deletion in a patient with Prader-Willi-Like phenotype and investigation of SIM1 gene deletion in 87 patients with sindromic obesity. Abstracts. 2005 ;[citado 2026 jan. 10 ] -
Vancouver
Varela MC, Kim CA, Bertola DR, Simões-Sato AY, Castro CIE, Koiffmann CP. A new case of interstitial 6q16.2 deletion in a patient with Prader-Willi-Like phenotype and investigation of SIM1 gene deletion in 87 patients with sindromic obesity. Abstracts. 2005 ;[citado 2026 jan. 10 ] - Angelman syndrome associated with oculocutaneous albinism due to an intragenic deletion of the P gene
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