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

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Monica Castro Varela

Centro de Estudos do Genoma Humano

Department of Biology

Institute of Biosciences

University of São Paulo

Brazil

[email]@ib.usp.br

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Affiliation

Centro de Estudos do Genoma Humano, Department of Biology, Institute of Biosciences, University of São Paulo, Brazil. 2004 - 2006

References

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 syndromic obesity. Varela, M.C., Simões-Sato, A.Y., Kim, C.A., Bertola, D.R., De Castro, C.I., Koiffmann, C.P. Eur. J. Med. Genet (2006) [Pubmed]
Impact of molecular mechanisms, including deletion size, on Prader-Willi syndrome phenotype: study of 75 patients. Varela, M.C., Kok, F., Setian, N., Kim, C.A., Koiffmann, C.P. Clin. Genet. (2005) [Pubmed]
Phenotypic variability in Angelman syndrome: comparison among different deletion classes and between deletion and UPD subjects. Varela, M.C., Kok, F., Otto, P.A., Koiffmann, C.P. Eur. J. Hum. Genet. (2004) [Pubmed]