Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: HARS2[original query] |
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Search for new loci and low-frequency variants influencing glioma risk by exome-array analysis. European journal of human genetics : EJHG 2015 Aug . Kinnersley Ben, Kamatani Yoichiro, Labussière Marianne, Wang Yufei, Galan Pilar, Mokhtari Karima, Delattre Jean-Yves, Gousias Konstantinos, Schramm Johannes, Schoemaker Minouk J, Swerdlow Anthony, Fleming Sarah J, Herms Stefan, Heilmann Stefanie, Nöthen Markus M, Simon Matthias, Sanson Marc, Lathrop Mark, Houlston Richard |
A Novel Missense Mutation in the CLPP Gene Causing Perrault Syndrome Type 3 in a Turkish Family. Journal of clinical research in pediatric endocrinology 2016 Apr . Dursun Fatma, Mohamoud Hussein Sheikh Ali, Karim Noreen, Naeem Muhammad, Jelani Musharraf, K?rm?z?bekmez Hev |
Whole-exome sequencing identifies rare pathogenic and candidate variants in sporadic Chinese Han deaf patients. Clinical genetics 2019 9 97 (2): 352-356. Zou Songfeng, Mei Xueshuang, Yang Weiqiang, Zhu Rvfei, Yang Tao, Hu Hong |
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