Items where Year is 2026

Article

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),