Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: PRMT2[original query] |
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Polymorphisms in DCDC2 and S100B associate with developmental dyslexia. Journal of human genetics 2015 Jul 60 (7): 399-401. Matsson Hans, Huss Mikael, Persson Helena, Einarsdottir Elisabet, Tiraboschi Ettore, Nopola-Hemmi Jaana, Schumacher Johannes, Neuhoff Nina, Warnke Andreas, Lyytinen Heikki, Schulte-Körne Gert, Nöthen Markus M, Leppänen Paavo Ht, Peyrard-Janvid Myriam, Kere Ju |
Autism spectrum disorder, anxiety and severe depression in a male patient with deletion and duplication in the 21q22.3 region: A case report. Biomedical reports 2019 7 1 (1): 1-5. Orru Sandro, Papoulidis Ioannis, Siomou Elisavet, Papadimitriou Dimitrios T, Sotiriou Sotirios, Nikolaidis Petros, Eleftheriades Makarios, Papanikolaou Evaggelos, Thomaidis Loretta, Manolakos Emmanou |
Specific Learning Disorders: Variation Analysis of 15 Candidate Genes in 9 Multiplex Families. Medicina (Kaunas, Lithuania) 2023 8 59 (8): . Francesco Calì, Francesco Domenico Di Blasi, Emanuela Avola, Mirella Vinci, Antonino Musumeci, Angelo Gloria, Donatella Greco, Daniela Rita Raciti, Alessandro Zagami, Biagio Rizzo, Santina Città, Concetta Federico, Luigi Vetri, Salvatore Saccone, Serafino Buo |
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