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[A patient with Pearson and Kearns-Sayre syndrome and a common 4.9 Kb deletion of mitochondrial DNA in blood].
An Esp Pediatr. 1998 Nov;49(5):510-2.
An Esp Pediatr. 1998.
PMID: 9949596
Spanish.
No abstract available.
[Familiar chronic progressive external ophthalmoplegia of mitochondrial origin].
Pineda M, Playán-Ariso A, Alcaine-Villarroya MJ, Vernet AM, Serra-Castanera A, Solano A, Vilaseca MA, Artuch R, López-Pérez M, Briones-Godino MP, Andreu A, Montoya J.
Pineda M, et al. Among authors: alcaine villarroya mj.
Rev Neurol. 2004 Jun 1-15;38(11):1023-7.
Rev Neurol. 2004.
PMID: 15202078
Free article.
Spanish.
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Phenotype in patients with intellectual disability and pathological results in array CGH.
Caballero Pérez V, López Pisón FJ, Miramar Gallart MD, González Álvarez A, García Jiménez MC, García Iñiguez JP, Orden Rueda C, Gil Hernández I, Fuertes Rodrigo C, Fernando Martínez R, Rodríguez Valle A, Alcaine Villarroya MJ.
Caballero Pérez V, et al. Among authors: alcaine villarroya mj.
Neurologia. 2017 Nov-Dec;32(9):568-578. doi: 10.1016/j.nrl.2016.03.006. Epub 2016 May 6.
Neurologia. 2017.
PMID: 27157524
Free article.
English, Spanish.
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