Search Results - PEREZ-GRANERO, Angeles

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  1. 1
    Atypical noncontiguous TSC2/PKD1 gene deletions presenting as tuberous sclerosis/polycystic kidney disease contiguous gene syndrome

    Atypical noncontiguous TSC2/PKD1 gene deletions presenting as tuberous sclerosis/polycystic kidney disease contiguous gene syndrome by Ventayol‐Guirado, Marc, Torres, Laura, Asensio‐Landa, Victor, Pérez‐Granero, Ángeles, Madrid, Maria Isabel, Hernandez‐Rodriguez, Jessica, Llull‐Alberti, Maria Victoria, Lumbreras, Javier, Escribà, Silvia, Pons, Monserrat, Roldan, Jordi, Martínez‐López, Iciar, Heine‐Suñer, Damian, Santos‐Simarro, Fernando

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  2. 2
    dup(1)(q21q32) as a sole cytogenetic event is associated to a leukemic transformation in Myelodysplastic Syndromes

    dup(1)(q21q32) as a sole cytogenetic event is associated to a leukemic transformation in Myelodysplastic Syndromes by Alfaro, Ramona, Pérez-Granero, Ángeles, Durán, Maria Antonia, Besalduch, Joan, Rosell, Jordi, Bernués, Marta

    Published in Leukemia research
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  3. 3
    Unrelated chromosomal anomalies found in patients with suspected 22q11.2 deletion

    Unrelated chromosomal anomalies found in patients with suspected 22q11.2 deletion by Fernández, Luis, Lapunzina, Pablo, López Pajares, Isidora, Palomares, María, Martínez, Isabel, Fernández, Blanca, Quero, José, García-Guereta, Luis, García-Alix, Alfredo, Burgueros, Margarita, Galán-Gómez, Enrique, Carbonell-Pérez, José María, Pérez-Granero, Ángeles, Torres-Juan, Laura, Heine-Suñer, Damià, Rosell, Jordi, Delicado, Alicia

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  4. 4
    Analysis of invdupdel(8p) rearrangement: Clinical, cytogenetic and molecular characterization

    Analysis of invdupdel(8p) rearrangement: Clinical, cytogenetic and molecular characterization by García-Santiago, Fe Amalia, Martínez-Glez, Víctor, Santos, Fernando, García-Miñaur, Sixto, Mansilla, Elena, Meneses, Antonio González, Rosell, Jordi, Granero, Ángeles Pérez, Vallespín, Elena, Fernández, Luis, Sierra, Blanca, Oliver-Bonet, María, Palomares, María, de Torres, María Luisa, Mori, María Ángeles, Nevado, Julián, Heath, Karen E., Delicado, Alicia, Lapunzina, Pablo

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  5. 5
    Unrelated Chromosomal Anomalies Found in Patients With Suspected 22qll.2 Deletion

    Unrelated Chromosomal Anomalies Found in Patients With Suspected 22qll.2 Deletion by FEMANDEZ, Luis, LAPUNZINA, Pablo, GALAN-GOMEZ, Enrique, CARBONELL-PEREZ, José Maria, PEREZ-GRANERO, Angeles, TORRES-JUAN, Laura, HEINE-SUNER, Damia, ROSELL, Jordi, DELICADO, Alicia, LOPEZ PAJARES, Isidora, PALOMARES, Maria, MARTINEZ, Isabel, FEMANDEZ, Blanca, QUERO, José, GARCIA-GUERETA, Luis, GARCIA-ALIX, Alfredo, BURGUEROS, Margarita

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  6. 6
    Variability in Phelan-McDermid Syndrome in a Cohort of 210 Individuals

    Variability in Phelan-McDermid Syndrome in a Cohort of 210 Individuals by Nevado, Julián, García-Miñaúr, Sixto, Palomares-Bralo, María, Vallespín, Elena, Guillén-Navarro, Encarna, Rosell, Jordi, Bel-Fenellós, Cristina, Mori, María Ángeles, Milá, Montserrat, Del Campo, Miguel, Barrúz, Pilar, Santos-Simarro, Fernando, Obregón, Gabriela, Orellana, Carmen, Pachajoa, Harry, Tenorio, Jair Antonio, Galán, Enrique, Cigudosa, Juan C, Moresco, Angélica, Saleme, César, Castillo, Silvia, Gabau, Elisabeth, Pérez-Jurado, Luis, Barcia, Ana, Martín, Maria Soledad, Mansilla, Elena, Vallcorba, Isabel, García-Murillo, Pedro, Cammarata-Scalisi, Franco, Gonçalves Pereira, Natálya, Blanco-Lago, Raquel, Serrano, Mercedes, Ortigoza-Escobar, Juan Dario, Gener, Blanca, Seidel, Verónica Adriana, Tirado, Pilar, Lapunzina, Pablo

    Published in Frontiers in genetics
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