ORIGINALES
Revisión de 22 casos de deleción 22q11.2: espectro fenotípico
Review of 22 patients with 22q11.2 deletion syndrome: phenotype spectrum
M.J. Ballesta Martíneza,
, E. Guillén Navarroa, I. López Expósitob, J.A. Bafalliu Vidalb, R. Domingo Jiménezc, J.M. Guía Torrentd, F. Robles Sáncheze, M. Sánchez Solís de Querolf
a Unidad de Genética Médica. Servicio de Pediatría. Murcia. España
b Sección de Citogenética. Centro de Bioquímica y Genética Clínica. Murcia. España
c Sección de Neuropediatría. Servicio de Pediatría. Hospital Universitario Virgen de la Arrixaca. Murcia. España
d Sección de Cardiología Infantil. Servicio de Pediatría. Hospital Universitario Virgen de la Arrixaca. Murcia. España
e Centro de Salud Mental de Molina. Murcia. España
f Sección de Neumología Infantil. Servicio de Pediatría. Hospital Universitario Virgen de la Arrixaca. Murcia. España
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Información del artículo
ISSN: 16954033Idioma original: Español
DOI:10.1157/13126553
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