Recurrence of Hirschsprung disease due to maternal mosaicism of a novel RET gene mutation by Amiñoso, C., García-Miñaúr, S., Martínez, L., Tenorio, J.A., Tovar, J.A., Lapunzina, P., Solera, J.

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Aberrant methylation of multiple genes in neuroblastic tumours: relationship with MYCN amplification and allelic status at 1p by Gonzalez-Gomez, P, Bello, M.J, Lomas, J, Arjona, D, Alonso, M.E, Amiñoso, C, Lopez-Marin, I, Anselmo, N.P, Sarasa, J.L, Gutierrez, M, Casartelli, C, Rey, J.A

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MLPA vs multiprobe FISH: comparison of two methods for the screening of subtelomeric rearrangements in 50 patients with idiopathic mental retardation by Palomares, M, Delicado, A, Lapunzina, P, Arjona, D, Amiñoso, C, Arcas, J, Martinez Bermejo, A, Fernández, L, López Pajares, I

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Factor H and CFHR1 polymorphisms associated with atypical Haemolytic Uraemic Syndrome (aHUS) are differently expressed in Tunisian and in Caucasian populations by Leban, N., Abarrategui-Garrido, C., Fariza-Requejo, E., Amiñoso-Carbonero, C., Pinto, S., Chibani, J. B., Khelil, A. H., Sánchez-Corral, P.

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Short Report: MLPA vs multiprobe FISH: comparison of two methods for the screening of subtelomeric rearrangements in 50 patients with idiopathic mental retardation by Palomares, M, Delicado, A, Lapunzina, P, Arjona, D, Amiñoso, C, Arcas, J, A Martinez Bermejo, Fernández, L, I López Pajares

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Molecular analysis of the EGFR gene in astrocytic gliomas: mRNA expression, quantitative-PCR analysis of non-homogeneous gene amplification and DNA sequence alterations by Arjona, D., Bello, M. J., Alonso, M. E., Aminoso, C., Isla, A., De Campos, J. M., Sarasa, J. L., Gutierrez, M., Villalobo, A., Rey, J. A.

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Genetic and epigenetic alteration of the NF2 gene in sporadic meningiomas by Lomas, Jesus, Bello, M. Josefa, Arjona, Dolores, Alonso, M. Eva, Martinez-Glez, Victor, Lopez-Marin, Isabel, Amiñoso, Cinthia, de Campos, Jose M., Isla, Alberto, Vaquero, Jesus, Rey, Juan A.

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Aberrant methylation of multiple genes in neuroblastic tumours by Gonzalez-Gomez, P, Bello, M.J, Lomas, J, Arjona, D, Alonso, M.E, Amiñoso, C, Lopez-Marin, I, Anselmo, N.P, Sarasa, J.L, Gutierrez, M, Casartelli, C, Rey, J.A

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DNA methylation of multiple promoter-associated CpG islands in meningiomas: relationship with the allelic status at 1p and 22q by Bello, M Josefa, Amiñoso, Cinthia, Lopez-Marin, Isabel, Arjona, Dolores, Gonzalez-Gomez, Pilar, Alonso, M Eva, Lomas, Jesus, de Campos, Jose M, Kusak, M Elena, Vaquero, Jesus, Isla, Alberto, Gutierrez, Manuel, Sarasa, Jose L, Rey, Juan A

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Recurrence of Hirschsprung disease due to maternal mosaicism of a novel RET gene mutation by Amiñoso, C, García-Miñaúr, S, Martínez, L, Tenorio, J A, Tovar, J A, Lapunzina, P, Solera, J

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Methylation status of TP73 in meningiomas by Lomas, Jesus, Amiñoso, Cinthia, Gonzalez-Gomez, Pilar, Eva Alonso, M, Arjona, Dolores, Lopez-Marin, Isabel, de Campos, Jose M, Isla, Alberto, Vaquero, Jesus, Gutierrez, Manuel, Sarasa, Jose L, Josefa Bello, M, Rey, Juan A

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CpG island methylation of tumor-related genes in three primary central nervous system lymphomas in immunocompetent patients by Gonzalez-Gomez, Pilar, Bello, M.Josefa, Arjona, Dolores, Alonso, M.Eva, Lomas, Jesus, Amiñoso, Cinthia, de Campos, Jose M., Sarasa, Jose L., Gutierrez, Manuel, Rey, Juan A.

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