Generation of induced pluripotent stem cells (iPSCs) by retroviral transduction of skin fibroblasts from four patients suffering Williams-Beuren syndrome (7q11.23 deletion) by Kuebler, B., Aran, B., Flores, R., Pérez-Jurado, L.A., Veiga, A., Corominas, R., Cuscó, I.

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Derivation of induced pluripotent stem cells (iPSCs) by retroviral transduction of skin fibroblasts from four patients suffering 7q11.23 microduplication syndrome by Kuebler, B., Aran, B., Flores, R., Pérez-Jurado, L.A., Veiga, A., Cuscó, I., Corominas, R.

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Síndrome de Bardet-Biedl: Aplicación diagnóstica de la secuenciación del exoma by Martos Moreno, G.Á, Rodríguez-Santiago, B, González Gutiérrez-Solana, L, Pérez-Jurado, L.A, Argente, J

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Quimerismo hemático en gemelos dicigóticos concebidos por fertilización in vitro by Martos-Moreno, G.Á, Campos, C, Flores, R, Yturriaga, R, Pérez-Jurado, L.A, Argente, J

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Clinical implication of FMR1 intermediate alleles in a Spanish population by Alvarez‐Mora, M.I., Madrigal, I., Martinez, F., Tejada, M.‐I., Izquierdo‐Alvarez, S., Sanchez‐Villar de Saz, P., Caro‐Llopis, A., Villate, O., Rodríguez‐Santiago, B., Pérez Jurado, L.A., Rodriguez‐Revenga, L., Milà, M.

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Evaluation of the Stag3 gene and the synaptonemal complex in a rat model (as/as) for male infertility by Bayés, Mònica, Prieto, I., Noguchi, J., Barbero, J.L., Jurado, L.A. Pérez

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Behavioral features of Williams Beuren syndrome compared to Fragile X syndrome and subjects with intellectual disability without defined etiology by Pérez-García, D., Granero, R., Gallastegui, F., Pérez-Jurado, L.A., Brun-Gasca, C.

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MAPT gene duplications are not a cause of frontotemporal lobar degeneration by Lladó, A., Rodríguez-Santiago, B., Antonell, A., Sánchez-Valle, R., Molinuevo, J.L., Reñé, R., Pérez-Jurado, L.A.

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Guía clínica para el seguimiento de pacientes con síndrome de Beckwith-Wiedemann by Lapunzina Badía, P., del Campo Casanelles, M., Delicado Navarro, A., Fernández-Toral, J., García-Alix, A., García-Guereta, L., Pérez Jurado, L.A., Ramos Fuentes, F.J., Sánchez Díaz, A., Urioste Azcorra, M.

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Genética no mendeliana y crecimiento. El síndrome de Russel-Silver by del Campo Casanelles, M., Pérez Jurado, L.A.

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Diabetes mellitus neonatal transitoria asociada a isodisomía uniparental del cromosoma 6 by Bonet Alcaina, M., García-Algar, O., Herrero Pérez, S., Pérez Jurado, L.A., Mombiela Vidal, R.

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Simple method for cystic fibrosis carrier screening by Molina Cabañera, J.C., Perez Jurado, L.A., Raskin, S., Vicario, J.L., Balas Perez, A., Garcia Novo, M.D.

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