Clinical description, molecular delineation and genotype–phenotype correlation in 340 patients with KBG syndrome: addition of 67 new patients
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Published in Journal of medical genetics (01.07.2023)
Published in Journal of medical genetics (01.07.2023)
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Mutations, Genes, and Phenotypes Related to Movement Disorders and Ataxias
Martínez-Rubio, Dolores, Hinarejos, Isabel, Sancho, Paula, Gorría-Redondo, Nerea, Bernadó-Fonz, Raquel, Tello, Cristina, Marco-Marín, Clara, Martí-Carrera, Itxaso, Martínez-González, María Jesús, García-Ribes, Ainhoa, Baviera-Muñoz, Raquel, Sastre-Bataller, Isabel, Martínez-Torres, Irene, Duat-Rodríguez, Anna, Janeiro, Patrícia, Moreno, Esther, Pías-Peleteiro, Leticia, Gordo, Mar O’Callaghan, Ruiz-Gómez, Ángeles, Muñoz, Esteban, Martí, Maria Josep, Sánchez-Monteagudo, Ana, Fuster, Candela, Andrés-Bordería, Amparo, Pons, Roser Maria, Jesús-Maestre, Silvia, Mir, Pablo, Lupo, Vincenzo, Pérez-Dueñas, Belén, Darling, Alejandra, Aguilera-Albesa, Sergio, Espinós, Carmen
Published in International journal of molecular sciences (01.10.2022)
Published in International journal of molecular sciences (01.10.2022)
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Isolated attention deficit disorder with/without hyperactivity in clinical practice. Series of cases
Marín Andrés, Marta, Gutiérrez Sánchez, Aída M, Martínez de Morentin Navarcorena, Ana L, Bernadó Fonz, Raquel A, Lafuente Hidalgo, Miguel, López Pisón, Javier
Published in Archivos argentinos de pediatría (01.08.2020)
Published in Archivos argentinos de pediatría (01.08.2020)
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