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Search on : RAMOS, E.S. [Author]
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 Magalhães, H.R. et al. Placental hydroxymethylation vsmethylation at the imprinting control region 2 on chromosome 11p15.5. Braz J Med Biol Res, Oct 2013, vol.46, no.11, p.916-919. ISSN 0100-879X
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 Araújo, A. and Ramos, E.S. Cryptic mosaicism involving a second chromosome X in patients with Turner syndrome. Braz J Med Biol Res, May 2008, vol.41, no.5, p.368-372. ISSN 0100-879X
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 Huber, J. and Ramos, E.S. The P48T germline mutation and polymorphism in the CDKN2A gene of patients with melanoma. Braz J Med Biol Res, Feb 2006, vol.39, no.2, p.237-241. ISSN 0100-879X
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 Ferreira, A.P.S. et al. Trisomy 13 mosaicism demonstrated only in skin fibroblasts in a patient presenting psychomotor retardation, pigmentary dysplasia and some dysmorphic features. Braz. J. Genet., 1996, vol.19, no.4, p.655-657. ISSN 0100-8455
    · abstract in english    · text in english


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