Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Epilepsy and DCX[original query] |
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The location of DCX mutations predicts malformation severity in X-linked lissencephaly. Neurogenetics 2008 Oct 9 (4): 277-85. Leger Pierre-Louis, Souville Isabelle, Boddaert Nathalie, Elie Caroline, Pinard Jean Marc, Plouin Perrine, Moutard Marie Laure, des Portes Vincent, Van Esch Hilde, Joriot Sylvie, Renard Jean Louis, Chelly Jamel, Francis Fiona, Beldjord Cherif, Bahi-Buisson Nad |
Targeted re-sequencing in malformations of cortical development: genotype-phenotype correlations. Seizure 2020 6 80 145-152. Accogli Andrea, Severino Mariasavina, Riva Antonella, Madia Francesca, Balagura Ganna, Iacomino Michele, Carlini Barbara, Baldassari Simona, Giacomini Thea, Croci Carolina, Pisciotta Livia, Messana Tullio, Boni Antonella, Russo Angelo, Bilo Leonilda, Tonziello Rosa, Coppola Antonietta, Filla Alessandro, Mecarelli Oriano, Casalone Rosario, Pisani Francesco, Falsaperla Raffaele, Marino Silvia, Parisi Pasquale, Ferretti Alessandro, Elia Maurizio, Luchetti Anna, Milani Donatella, Vanadia Francesca, Silvestri Laura, Rebessi Erika, Parente Eliana, Vatti Giampaolo, Mancardi Maria Margherita, Nobili Lino, Capra Valeria, Salpietro Vincenzo, Striano Pasquale, Zara Federi |
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