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 Cammarata-Scalisi, Francisco et al. Síndrome de Beckwith-Wiedemann: Aspectos clínicos y etiopatogénicos de una entidad ejemplo de impronta genómica. Arch. argent. pediatr., Oct 2018, vol.116, no.5, p.368-373. ISSN 0325-0075

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 Cammarata-Scalisi, Francisco et al. Trisomía 18 en mosaico: Serie de casos. Arch. argent. pediatr., Jun 2017, vol.115, no.3, p.e183-e186. ISSN 0325-0075

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 Cammarata-Scalisi, Francisco et al. Alelo doble mutante en el gen EXT1 no informado previamente en una adolescente con exostosis múltiple hereditaria. Arch. argent. pediatr., Abr 2015, vol.113, no.2, p.e109-e112. ISSN 0325-0075
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