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MULTI-OMICS CHARACTERIZATION OF NEURODEVELOPMENTAL DISORDERS by Katia Sofia Illescas, Guerau Fernández Isern, Alfonso Oyarzábal, Àngels García-Cazorla
Published 2023-10-01
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Coexistence of junctional epidermolysis bullosa, autosomal recessive deafness type 57, and Angelman syndrome: A case report by Maria Eugenia Amato, Silvia Ricart, Maria Asunción Vicente, Loreto Martorell, Judith Armstrong, Guerau Fernández Isern, José Manuel Mascaro, Sol Balsells, Itziar Alonso, Mercedes Serrano, Juan Darío Ortigoza‐Escobar
Published 2023-04-01
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