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Cammarata-Scalisi, Francisco et al. Clinical and genetic findings of two cases with Apert syndrome. Bol. Med. Hosp. Infant. Mex., Feb 2019, vol.76, no.1, p.44-48. ISSN 1665-1146

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Cammarata-Scalisi, Francisco et al. Hallazgos clínicos y epidemiológicos en la neurofibromatosis tipo 1 y el complejo esclerosis tuberosa en una serie de pacientes pediátricos. Bol. Med. Hosp. Infant. Mex., Oct 2018, vol.75, no.5, p.287-294. ISSN 1665-1146

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