Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: CHN1[original query] |
---|
A microdeletion in the GRHL2 Gene in two unrelated patients with congenital fibrosis of the extra ocular muscles. BMC research notes 2017 Nov 10 (1): 562. Abu-Amero Khaled K, Kondkar Altaf A, Khan Arif |
Genome-wide interaction study of gene-by-occupational exposures on respiratory symptoms. Environment international 2019 01 122 263-269. Zeng Xiang, Vonk Judith M, van der Plaat Diana A, Faiz Alen, Paré Peter D, Joubert Philippe, Nickle David, Brandsma Corry-Anke, Kromhout Hans, Vermeulen Roel, Xu Xijin, Huo Xia, de Jong Kim, Boezen H Mari |
Clinical and genetic characteristics of Chinese patients with congenital cranial dysinnervation disorders. Orphanet journal of rare diseases 2022 12 17 (1): 431. Jia Hongyan, Ma Qian, Liang Yi, Wang Dan, Chang Qinglin, Zhao Bo, Zhang Zongrui, Liang Jing, Song Jing, Wang Yidi, Zhang Ranran, Tu Zhanhan, Jiao Yongho |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: