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Cammarata-Scalisi, Francisco et al.
Síndrome de Beckwith-Wiedemann: Aspectos clínicos y etiopatogénicos de una entidad ejemplo de impronta genómica
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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
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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
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Arch. argent. pediatr.
, Abr 2015, vol.113, no.2, p.e109-e112. ISSN 0325-0075
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