Items where Year is 2026

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Marianski, Krzysztof, Talcott, Joel B., Stein, John, Monaco, Anthony P., Fisher, Simon E., Bishop, Dorothy V. M., Newbury, Dianne F. and Paracchini, Silvia (2026). Whole-exome sequencing in children with dyslexia implicates rare variants in CLDN3 and ion channel genes. Human Genetics, 145 (2),