Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Syndrome and LRP4[original query] |
---|
A variant of the LRP4 gene affects the risk of chronic lymphocytic leukaemia transformation to Richter syndrome. British journal of haematology 2010 Dec . Rasi S, Spina V, Bruscaggin A, Vaisitti T, Tripodo C, Forconi F, De Paoli L, Fangazio M, Sozzi E, Cencini E, Laurenti L, Marasca R, Visco C, Xu-Monette ZY, Gattei V, Young KH, Malavasi F, Deaglio S, Gaidano G, Rossi D |
No mutations in the serotonin related TPH1 and HTR1B genes in patients with monogenic sclerosing bone disorders. Bone 2013 Jul 55 (1): 52-6. Boudin Eveline, Jennes Karen, de Freitas Fenna, Tegay David, Mortier Geert, Van Hul W |
Mutations in the fourth ?-propeller domain of LRP4 are associated with isolated syndactyly with fusion of the third and fourth fingers. Human mutation 2018 3 39 (6): 811-815. Sukenik Halevy Rivka, Chien Huan-Chieh, Heinz Bo, Bamshad Michael J, Nickerson Deborah A, , Kircher Martin, Ahituv Nad |
- Page last reviewed:Feb 1, 2024
- Content source: