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 Cammarata-Scalisi, Francisco et al. Síndrome de Wolf-Hirschhorn: Descripción de cinco casos caracterizados por microarrays de polimorfismos de nucleótido único. Arch. argent. pediatr., Ago 2019, vol.117, no.4, p.e406-e412. ISSN 0325-0075


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 Cammarata-Scalisi, Francisco et al. Hallazgos clínicos, bioquímicos y moleculares de la acidemia propiónica. Arch. argent. pediatr., Jun 2019, vol.117, no.3, p.e288-e291. ISSN 0325-0075


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 Callea, Michele et al. Estudio dínico y molecular en una familia con displasia cleidocraneal. Arch. argent. pediatr., Dic 2017, vol.115, no.6, p.e440-e444. 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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