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Database :	article
Search on :	CAMMARATA-SCALISI, FRANCISCO [Author]
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Cammarata-Scalisi, Francisco. Trisomía 9p: Una breve descripción clínica, diagnóstica y terapéutica. Arch. argent. pediatr., Oct 2019, vol.117, no.5, p.e473-e476. ISSN 0325-0075

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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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Cammarata-Scalisi, Francisco, Avendaño, Andrea and Called, Michele Principales entidades genéticas asociadas con dientes supernumerarios. Arch. argent. pediatr., Dic 2018, vol.116, no.6, p.437-444. ISSN 0325-0075

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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. Embriopatía por isotretinoína: Una entidad que puede evitarse. Arch. argent. pediatr., Abr 2018, vol.116, no.2, p.e303-e307. 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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Callea, Michele et al. Estudio dínico y molecular en una familia con displasia ectodermica hipohidrotica autosomica dominante. Arch. argent. pediatr., Feb 2017, vol.115, no.1, p.e34-e38. ISSN 0325-0075

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Callea, Michele et al. Estudio clínico y molecular en un escolar con displasia ectodérmica hipohidrótica ligada al X. Arch. argent. pediatr., Dic 2015, vol.113, no.6, p.e341-e344. ISSN 0325-0075

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