Search Results - Plaja, Alberto

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  1. 1
    LRBA Deficiency in a Patient With a Novel Homozygous Mutation Due to Chromosome 4 Segmental Uniparental Isodisomy

    LRBA Deficiency in a Patient With a Novel Homozygous Mutation Due to Chromosome 4 Segmental Uniparental Isodisomy by Soler-Palacín, Pere, Garcia-Prat, Marina, Martín-Nalda, Andrea, Franco-Jarava, Clara, Rivière, Jacques G., Plaja, Alberto, Bezdan, Daniela, Bosio, Mattia, Martínez-Gallo, Mónica, Ossowski, Stephan, Colobran, Roger

    Published 2018
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  2. 2
    Assessment of QF-PCR as the First Approach in Prenatal Diagnosis

    Assessment of QF-PCR as the First Approach in Prenatal Diagnosis by Badenas, Celia, Rodríguez-Revenga, Laia, Morales, Carme, Mediano, Carmen, Plaja, Alberto, Pérez-Iribarne, Ma Mar, Soler, Anna, Clusellas, Núria, Borrell, Antoni, Sánchez, Ma Ángeles, Miró, Elisabeth, Sánchez, Aurora, Milà, Montserrat, Jiménez, Wladimiro

    Published 2010
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  3. 3
    Novel Double Factor PGT strategy analyzing blastocyst stage embryos in a single NGS procedure

    Novel Double Factor PGT strategy analyzing blastocyst stage embryos in a single NGS procedure by del Rey, Javier, Vidal, Francisco, Ramírez, Lorena, Borràs, Nina, Corrales, Irene, Garcia, Iris, Martinez-Pasarell, Olga, Fernandez, Silvia F., Garcia-Cruz, Raquel, Pujol, Aïda, Plaja, Alberto, Salaverria, Itziar, Oliver-Bonet, Maria, Benet, Jordi, Navarro, Joaquima

    Published 2018
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  4. 4
    Tumour selection advantage of non‐dominant negative P53 mutations in homozygotic MDM2‐SNP309 colorectal cancer cells

    Tumour selection advantage of non‐dominant negative P53 mutations in homozygotic MDM2‐SNP309 colorectal cancer cells by Alazzouzi, Hafid, Suriano, Gianpaolo, Guerra, Angel, Plaja, Alberto, Espín, Eloi, Armengol, Manel, Alhopuro, Pia, Velho, Sergia, Shinomura, Yasuhisa, González‐Aguilera, Juan José, Yamamoto, Hiroyuki, Aaltonen, Lauri A, Moreno, Víctor, Capellà, Gabriel, Peinado, Miguel Angel, Seruca, Raquel, Arango, Diego

    Published 2007
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  5. 5
    Clinical utility of chromosomal microarray analysis in invasive prenatal diagnosis

    Clinical utility of chromosomal microarray analysis in invasive prenatal diagnosis by Armengol, Lluís, Nevado, Julián, Serra-Juhé, Clara, Plaja, Alberto, Mediano, Carmen, García-Santiago, Fe Amalia, García-Aragonés, Manel, Villa, Olaya, Mansilla, Elena, Preciado, Cristina, Fernández, Luis, Mori, María Ángeles, García-Pérez, Lidia, Lapunzina, Pablo Daniel, Pérez-Jurado, Luis Alberto

    Published 2011
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  6. 6
    PIAS4 is associated with macro/microcephaly in the novel interstitial 19p13.3 microdeletion/microduplication syndrome

    PIAS4 is associated with macro/microcephaly in the novel interstitial 19p13.3 microdeletion/microduplication syndrome by Nevado, Julián, Rosenfeld, Jill A, Mena, Rocío, Palomares-Bralo, María, Vallespín, Elena, Ángeles Mori, María, Tenorio, Jair A, Gripp, Karen W, Denenberg, Elizabeth, del Campo, Miguel, Plaja, Alberto, Martín-Arenas, Rubén, Santos-Simarro, Fernando, Armengol, Lluis, Gowans, Gordon, Orera, María, Sanchez-Hombre, M Carmen, Corbacho-Fernández, Esther, Fernández-Jaén, Alberto, Haldeman-Englert, Chad, Saitta, Sulagna, Dubbs, Holly, Bénédicte, Duban B, Li, Xia, Devaney, Lani, Dinulos, Mary Beth, Vallee, Stephanie, Crespo, M Carmen, Fernández, Blanca, Fernández-Montaño, Victoria E, Rueda-Arenas, Inmaculada, de Torres, María Luisa, Ellison, Jay W, Raskin, Salmo, Venegas-Vega, Carlos A, Fernández-Ramírez, Fernando, Delicado, Alicia, García-Miñaúr, Sixto, Lapunzina, Pablo

    Published 2015
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