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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

Sergio Alberto Cuevas-Covarrubias

Servicio de Genética

Hospital General de México

Facultad de Medicina

Universidad Nacional Autónoma de México



Name/email consistency: high



  • Servicio de Genética, Hospital General de México, Facultad de Medicina, Universidad Nacional Autónoma de México, Mexico. 2002 - 2008


  1. Analysis of the VCX3A, VCX2 and VCX3B genes shows that VCX3A gene deletion is not sufficient to result in mental retardation in X-linked ichthyosis. Cuevas-Covarrubias, S.A., González-Huerta, L.M. Br. J. Dermatol. (2008) [Pubmed]
  2. Somatic and germinal mosaicism for the steroid sulfatase gene deletion in a steroid sulfatase deficiency carrier. Cuevas-Covarrubias, S.A., Jiménez-Vaca, A.L., González-Huerta, L.M., Valdes-Flores, M., Del Refugio Rivera-Vega, M., Maya-Nunez, G., Kofman-Alfaro, S.H. J. Invest. Dermatol. (2002) [Pubmed]
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