Journal Information
Vol. 58. Issue 5.
Pages 506-507 (1 May 2003)
Vol. 58. Issue 5.
Pages 506-507 (1 May 2003)
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Foramina parietalia permagna, un raro defecto congénito
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A. Blanco del Val
Corresponding author
ablancoval@navegalia.com

Secretaría del Servicio de Pediatría. Hospital Universitario Río Hortega. Cardenal Torquemada, s/n. 47010 Valladolid. España.
, M.I. Carrascal Arranz, F. Centeno Malfaz, H. Marcos Andrés, C. Alcalde Martín
Servicio de Pediatría. Hospital Universitario Río Hortega. Valladolid. España.
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Bibliografía
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The AWL4 homeobox gene is mutated in patients with ossification defect of the skull (foramina parietalia permagna, OMIM 168500).
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Copyright © 2003. Asociación Española de Pediatría
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