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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 20, 2025. (Total: 235500Documents)
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Records 1 - 2 (of 2 Records)

Query Trace: Fibrosis and 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
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
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