Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: MYO18B[original query] |
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Fine mapping of chromosome 22q tumor suppressor gene candidate regions in astrocytoma. International journal of cancer 2004 1 108 (6): 839-44. Hartmann Christian, Nümann Astrid, Mueller Wolf, Holtkamp Nikola, Simon Matthias, von Deimling Andre |
A population-specific uncommon variant in GRIN3A associated with schizophrenia. Biological psychiatry 2012 Dec . Takata A, Iwayama Y, Fukuo Y, Ikeda M, Okochi T, Maekawa M, Toyota T, Yamada K, Hattori E, Ohnishi T, Toyoshima M, Ujike H, Inada T, Kunugi H, Ozaki N, Nanko S, Nakamura K, Mori N, Kanba S, Iwata N, Kato T, Yoshikawa T |
Ethnic specificity of lupus-associated loci identified in a genome-wide association study in Korean women. Annals of the rheumatic diseases 2014 Jun 73 (6): 1240-5. Lee Hye-Soon, Kim Taehyeung, Bang So Young, Na Young Ji, Kim Il, Kim Kwangwoo, Kim Jae-Hoon, Chung Yeun-Jun, Shin Hyoung Doo, Kang Young Mo, Shim Seung-Cheol, Suh Chang-Hee, Park Yong-Beom, Kim Jong-Sung, Kang Changwon, Bae Sang-Che |
A common variant in myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults.
Translational psychiatry 2013 3 e229. Ludwig K U, Sämann P, Alexander M, Becker J, Bruder J, Moll K, Spieler D, Czisch M, Warnke A, Docherty S J, Davis O S P, Plomin R, Nöthen M M, Landerl K, Müller-Myhsok B, Hoffmann P, Schumacher J, Schulte-Körne G, Czamara |
Characterization of germline mutations in familial lung cancer from the Chinese population. Gene 2017 Oct . Kanwal Madiha, Ding Xiao-Jie, Ma Zhans-Han, Li Lian-Wei, Wang Ping, Chen Ying, Huang Yun-Chao, Cao |
The mutational burden and oligogenic inheritance in Klippel-Feil syndrome. BMC musculoskeletal disorders 2020 Apr 21 (1): 220. Li Ziquan, Zhao Sen, Cai Siyi, Zhang Yuanqiang, Wang Lianlei, Niu Yuchen, Li Xiaoxin, Hu Jianhua, Chen Jingdan, Wang Shengru, Wang Huizi, Liu Gang, Tian Ye, Wu Zhihong, Zhang Terry Jianguo, , Wang Yipeng, Wu N |
[Clinical Characteristics and Genetic Analysis of Klippel-Feil Syndrome]. Zhongguo yi xue ke xue yuan xue bao. Acta Academiae Medicinae Sinicae 2021 3 43 (1): 25-31. Li Zi Quan, Geng Mo Zhao, Zhao Sen, Wu Zhi Hong, Zhang Jian Guo, Wu Nan, Wang Yi Pe |
Genome-wide association study identifies 18 novel loci associated with left atrial volume and function.
European heart journal 2021 8 . Ahlberg Gustav, Andreasen Laura, Ghouse Jonas, Bertelsen Litten, Bundgaard Henning, Haunsø Stig, Svendsen Jesper H, Olesen Morten |
Genetic diagnosis of fetal microcephaly at a single tertiary center in China. Frontiers in genetics 2023 5 14 1112153. You Wang, Fang Fu, Tingying Lei, Li Zhen, Qiong Deng, Hang Zhou, Chunling Ma, Ken Cheng, Ruibin Huang, Ru Li, Qiuxia Yu, Lushan Li, Jin Han, Xin Yang, Dongzhi Li, Can Li |
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- Page last updated:Apr 22, 2024
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