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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Syndrome and SRCAP[original query]
Ultra-rare mutations in SRCAP segregate in Caribbean Hispanic families with Alzheimer disease.
Neurology. Genetics 2017 Oct 3 (5): e178.
Vardarajan Badri N, Tosto Giuseppe, Lefort Roger, Yu Lei, Bennett David A, De Jager Philip L, Barral Sandra, Reyes-Dumeyer Dolly, Nagy Peter L, Lee Joseph H, Cheng Rong, Medrano Martin, Lantigua Rafael, Rogaeva Ekaterina, St George-Hyslop Peter, Mayeux Richa
Novel genotypes and phenotypes among Chinese patients with Floating-Harbor syndrome.
Orphanet journal of rare diseases 2019 Jun 14 (1): 144.
Zhang Shujie, Chen Shaoke, Qin Haisong, Yuan Haiming, Pi Yalei, Yang Yu, Huang Hui, Li Guimei, Sun Yan, Wang Zhihua, Ma Huamei, Fu Xiaoling, Zhou Ting, Wang Jian, Zhang Huifeng, Shen Yipi
Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients.
Clinical epigenetics 2020 6 12 (1): 86.
Inoue Takanobu, Nakamura Akie, Iwahashi-Odano Megumi, Tanase-Nakao Kanako, Matsubara Keiko, Nishioka Junko, Maruo Yoshihiro, Hasegawa Yukihiro, Suzumura Hiroshi, Sato Seiji, Kobayashi Yoshiyuki, Murakami Nobuyuki, Nakabayashi Kazuhiko, Yamazawa Kazuki, Fuke Tomoko, Narumi Satoshi, Oka Akira, Ogata Tsutomu, Fukami Maki, Kagami Masa
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