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[Catch-22: current implication of the microdeletion in 22q11].
del Campo Casanelles M, Pérez Rodríguez J, García Guereta L, Delicado A, Quero Jiménez J. del Campo Casanelles M, et al. An Esp Pediatr. 1996 Oct;45(4):341-5. An Esp Pediatr. 1996. PMID: 9005718 Review. Spanish. No abstract available.
Unrelated chromosomal anomalies found in patients with suspected 22q11.2 deletion.
Fernández L, Lapunzina P, Pajares IL, Palomares M, Martínez I, Fernández B, Quero J, García-Guereta L, García-Alix A, Burgueros M, Galán-Gómez E, Carbonell-Pérez JM, Pérez-Granero A, Torres-Juan L, Heine-Suñer D, Rosell J, Delicado A. Fernández L, et al. Am J Med Genet A. 2008 May 1;146A(9):1134-41. doi: 10.1002/ajmg.a.32256. Am J Med Genet A. 2008. PMID: 18384142
Molecular and histologic insights on early onset cardiomyopathy in Danon disease females.
Fernández L, Casamayor Polo L, Bravo García-Morato M, Enguita Valls AB, Ruiz-Bravo E, Muñoz-Cabello P, Ibáñez K, Rodríguez-Laguna L, Martín-Arenas R, Ortega M, Palomares-Bralo M, Del Pozo Á, García-Guereta L, García-Miñaúr S, Lapunzina P, Vallespín E. Fernández L, et al. Clin Genet. 2021 Mar;99(3):481-483. doi: 10.1111/cge.13884. Epub 2020 Nov 23. Clin Genet. 2021. PMID: 33226119 No abstract available.
[Clinical guide to the management of patients with Beckwith-Wiedemann syndrome].
Lapunzina Badía P, del Campo Casanelles M, Delicado Navarro A, Fernández-Toral J, García-Alix A, García-Guereta L, Pérez Jurado LA, Ramos Fuentes FJ, Sánchez Díaz A, Urioste Azcorra M. Lapunzina Badía P, et al. An Pediatr (Barc). 2006 Mar;64(3):252-9. doi: 10.1157/13085513. An Pediatr (Barc). 2006. PMID: 16527093 Free article. Spanish.
[Congenital and post-operative chylothorax in the neonatal period].
González de Dios J, García Martín B, Burgueros Valero M, García Guereta L, Borches Jacassa D, Pérez Rodríguez J, Quero Jiménez J. González de Dios J, et al. An Esp Pediatr. 1992 Feb;36(2):109-14. An Esp Pediatr. 1992. PMID: 1575397 Review. Spanish.
73 results