Dominant-negative kinase domain mutations in FGFR1 can explain the clinical severity of Hartsfield syndrome - Hong, Sungkook; Hu, Ping; Marino, Juliana; Hufnagel, Sophia B.; Hopkin, Robert J.; Toromanovic, Alma; Richieri-Costa, Antonio; Bicudo, Lucilene A. Ribeiro; Kruszka, Paul; Roessler, Erich; Muenke, Maximilian (Human Molecular Genetics, 2016)