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Revista De Neurologia|February 9, 2012
[X-chromosome-linked ichthyosis associated to epilepsy, hyperactivity, autism and mental retardation, due to the Xp22.31 microdeletion]M Carmen Carrascosa-Romero, Javier Suela, Blanca Alfaro-Ponce, et al.
Journal of Immunology (Baltimore, Md. : 1950)|June 10, 2004
Expression of human CD1d molecules protects target cells from NK cell-mediated cytolysisYolanda Campos-Martín, Manuel Gómez del Moral, Beatriz Gozalbo-López, et al.
American Journal of Medical Genetics. Part A|March 13, 2012
Neonatal detection of 5p13.2 duplication and delineation of the phenotypeM Carmen Carrascosa Romero, Rosa García Hoyo, María Calvente, et al.
BMC Cancer|January 2, 2023
Differential presence of exons (DPE): sequencing liquid biopsy by NGS. A new method for clustering colorectal Cancer patientsDavid Rubio-Mangas, Mariano García-Arranz, Yaima Torres-Rodriguez, et al.
Advances in Laboratory Medicine|June 26, 2023
Prenatal screening and diagnosis of genetic abnormalities: SEGO, SEQC<sup>ML</sup>, AEDP consensus recommendationsBelén Prieto, Begoña Adiego, Javier Suela, et al.
Haematologica|June 7, 2007
Multiple myeloma primary cells show a highly rearranged unbalanced genome with amplifications and homozygous deletions irrespective of the presence of immunoglobulin-related chromosome translocationsCristina Largo, Borja Saéz, Sara Alvarez, et al.
Genes, Chromosomes & Cancer|January 17, 2016
Guidelines for genomic array analysis in acquired haematological neoplastic disordersJacqueline Schoumans, Javier Suela, Ros Hastings, et al.
DNA Repair|May 2, 2017
Polμ deficiency induces moderate shortening of P53<sup>-/-</sup> mouse lifespan and modifies tumor spectrumBeatriz Escudero, Diego Herrero, Yaima Torres, et al.
Revista De Neurologia|September 26, 2014
[Genetics applied to clinical practice in neurodevelopmental disorders]Alberto Fernández-Jaén, Juan C Cigudosa, Daniel Martín Fernández-Mayoralas, et al.
Journal of Translational Medicine|August 7, 2013
Identification of prefoldin amplification (1q23.3-q24.1) in bladder cancer using comparative genomic hybridization (CGH) arrays of urinary DNAVirginia López, Pilar González-Peramato, Javier Suela, et al.
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