Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Death and MEF2C[original query] |
---|
Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness.
BMC medical genetics 2007 8 Suppl 1 S3. Levy Daniel, Larson Martin G, Benjamin Emelia J, Newton-Cheh Christopher, Wang Thomas J, Hwang Shih-Jen, Vasan Ramachandran S, Mitchell Gary |
Clinical and molecular characteristics of MEF2D fusion-positive B-cell precursor acute lymphoblastic leukemia in childhood, including a novel translocation resulting in MEF2D-HNRNPH1 gene fusion. Haematologica 2018 9 104 (1): 128-137. Ohki Kentaro, Kiyokawa Nobutaka, Saito Yuya, Hirabayashi Shinsuke, Nakabayashi Kazuhiko, Ichikawa Hitoshi, Momozawa Yukihide, Okamura Kohji, Yoshimi Ai, Ogata-Kawata Hiroko, Sakamoto Hiromi, Kato Motohiro, Fukushima Keitaro, Hasegawa Daisuke, Fukushima Hiroko, Imai Masako, Kajiwara Ryosuke, Koike Takashi, Komori Isao, Matsui Atsushi, Mori Makiko, Moriwaki Koichi, Noguchi Yasushi, Park Myoung-Ja, Ueda Takahiro, Yamamoto Shohei, Matsuda Koichi, Yoshida Teruhiko, Matsumoto Kenji, Hata Kenichiro, Kubo Michiaki, Matsubara Yoichi, Takahashi Hiroyuki, Fukushima Takashi, Hayashi Yasuhide, Koh Katsuyoshi, Manabe Atsushi, Ohara Akira, |
ISL1 loss-of-function variation causes familial atrial fibrillation. European journal of medical genetics 2020 8 63 (11): 104029. Wu Shao-Hui, Wang Xin-Hua, Xu Ying-Jia, Gu Jia-Ning, Yang Chen-Xi, Qiao Qi, Guo Xiao-Juan, Guo Yu-Han, Qiu Xing-Biao, Jiang Wei-Feng, Yang Yi-Qi |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: