Genome-wide CNV investigation in systemic Lupus erythematosus patients reveals CNV predominance on the X chromosome (2013)
- Authors:
- USP affiliated authors: DONADI, EDUARDO ANTONIO - FMRP ; SIMÕES, AGUINALDO LUIZ - FMRP
- Unidade: FMRP
- Subjects: LÚPUS ERITEMATOSO SISTÊMICO; GENOMAS
- Language: Inglês
- Imprenta:
- Publisher: SBG
- Publisher place: Águas de Lindóia
- Date published: 2013
- Source:
- Título: Abstracts
- Conference titles: Congresso Brasileiro de Genética
-
ABNT
BARBOSA, F. B. et al. Genome-wide CNV investigation in systemic Lupus erythematosus patients reveals CNV predominance on the X chromosome. 2013, Anais.. Águas de Lindóia: SBG, 2013. . Acesso em: 11 fev. 2026. -
APA
Barbosa, F. B., Simioni, M., Donadi, E. A., Silva-Lopes, V. L. G. da, & Simões, A. L. (2013). Genome-wide CNV investigation in systemic Lupus erythematosus patients reveals CNV predominance on the X chromosome. In Abstracts. Águas de Lindóia: SBG. -
NLM
Barbosa FB, Simioni M, Donadi EA, Silva-Lopes VLG da, Simões AL. Genome-wide CNV investigation in systemic Lupus erythematosus patients reveals CNV predominance on the X chromosome. Abstracts. 2013 ;[citado 2026 fev. 11 ] -
Vancouver
Barbosa FB, Simioni M, Donadi EA, Silva-Lopes VLG da, Simões AL. Genome-wide CNV investigation in systemic Lupus erythematosus patients reveals CNV predominance on the X chromosome. Abstracts. 2013 ;[citado 2026 fev. 11 ] - Ancestry informative marker panel to estimate population stratification using genome-wide human array
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- Padrão de desequilíbrio de ligação gênica em SNPs candidatos à associação ao Lúpus Eritematoso Sistêmico
- CNV profile is systemic Lupus erythematosus patients
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- Genetic susceptibility factors in MHC associated with psoriasis vulgaris: a study of brazilian patients
- Absence of the HLA-G*0105N allele in Amerindian populations from the Brazilian Amazon Region: a possible role of natural selection
- Diversity of the region 3'UTR of gene HLA-G in the urban population of the state of São Paulo and amerindian of the brazilian amazon
- Detection of rare copy number variants in patients with systemic lupus erythematosus
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