Identification of SHOX deletion in patients with disproportional short stature or Léri-Weill dyschodrosteosis: comparison between the fluorescence in situ hybridization technique and microsatellite study (2007)
- Authors:
- Autor USP: MENDONÇA, BERENICE BILHARINHO DE - FM
- Unidade: FM
- Subjects: DELEÇÃO DE GENES; FLUORESCÊNCIA; HIBRIDIZAÇÃO; DESENVOLVIMENTO FÍSICO; CRESCIMENTO E DESENVOLVIMENTO (FISIOPATOLOGIA); RESUMOS (SIMPÓSIOS)
- Language: Inglês
- Imprenta:
- Source:
- Conference titles: Simpósio avanços em pesquisas médicas
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ABNT
FUNARI, M. F. et al. Identification of SHOX deletion in patients with disproportional short stature or Léri-Weill dyschodrosteosis: comparison between the fluorescence in situ hybridization technique and microsatellite study. Clinics. São Paulo: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 23 abr. 2024. , 2007 -
APA
Funari, M. F., Jorge, A. A. L., Souza, S. C., Mendonça, B. B. de, & Nishi, M. Y. (2007). Identification of SHOX deletion in patients with disproportional short stature or Léri-Weill dyschodrosteosis: comparison between the fluorescence in situ hybridization technique and microsatellite study. Clinics. São Paulo: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Funari MF, Jorge AAL, Souza SC, Mendonça BB de, Nishi MY. Identification of SHOX deletion in patients with disproportional short stature or Léri-Weill dyschodrosteosis: comparison between the fluorescence in situ hybridization technique and microsatellite study. Clinics. 2007 ; 62 S87.[citado 2024 abr. 23 ] -
Vancouver
Funari MF, Jorge AAL, Souza SC, Mendonça BB de, Nishi MY. Identification of SHOX deletion in patients with disproportional short stature or Léri-Weill dyschodrosteosis: comparison between the fluorescence in situ hybridization technique and microsatellite study. Clinics. 2007 ; 62 S87.[citado 2024 abr. 23 ] - Variable ACTH-stimulated 17-Hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations
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