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Cromosomopatía con anillación del 21 (r21) y epilepsia / Chromosome 21 ring (r21) and epilepsy
Pardal Fernández, JM; Pérez García, P; Carrascosa Romero, MC; Marco Giner, J.
Affiliation
  • Pardal Fernández, JM; Hospital General Universiario de Albacete. Servicio de Neurofisiología Clínica. Albacete. España
  • Pérez García, P; Hospital General Universiario de Albacete. Servicio de Neurofisiología Clínica. Albacete. España
  • Carrascosa Romero, MC; Hospital General Universiario de Albacete. Sección de Neuropediatría. Albacete. España
  • Marco Giner, J; Hospital General Universiario de Albacete. Servicio de Neurofisiología Clínica. Albacete. España
An. pediatr. (2003, Ed. impr.) ; 60(4): 379-381, abr. 2004.
Article in Es | IBECS | ID: ibc-31647
Responsible library: ES1.1
Localization: ES1.1 - BNCS
RESUMEN
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Subject(s)
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Collection: National databases / Spain Database: IBECS Main subject: Phenotype / Abnormalities, Multiple / Chromosomes, Human, Pair 21 / Epilepsy Limits: Humans / Male / Infant, Newborn Language: Spanish Journal: An. pediatr. (2003, Ed. impr.) Year: 2004 Document type: Article Institution/Affiliation country: Hospital General Universiario de Albacete/España
Search on Google
Add to My VHL
Print
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Collection: National databases / Spain Database: IBECS Main subject: Phenotype / Abnormalities, Multiple / Chromosomes, Human, Pair 21 / Epilepsy Limits: Humans / Male / Infant, Newborn Language: Spanish Journal: An. pediatr. (2003, Ed. impr.) Year: 2004 Document type: Article Institution/Affiliation country: Hospital General Universiario de Albacete/España