Human Genome Epidemiology Literature Finder
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Records 1 - 3 (of 3 Records) |
| Query Trace: Disease and ARF6[original query] |
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| A syndrome of congenital microcephaly, intellectual disability and dysmorphism with a homozygous mutation in FRMD4A. European journal of human genetics : EJHG 2014 Nov . Fine Dina, Flusser Hagit, Markus Barak, Shorer Zamir, Gradstein Libe, Khateeb Shareef, Langer Yshia, Narkis Ginat, Birk Ruth, Galil Aharon, Shelef Ilan, Birk Ohad |
| C1orf106 is a colitis risk gene that regulates stability of epithelial adherens junctions. Science (New York, N.Y.) 2018 Feb . Mohanan Vishnu, Nakata Toru, Desch A Nicole, Lévesque Chloé, Boroughs Angela, Guzman Gaelen, Cao Zhifang, Creasey Elizabeth, Yao Junmei, Boucher Gabrielle, Charron Guy, Bhan Atul K, Schenone Monica, Carr Steven A, Reinecker Hans-Christian, Daly Mark J, Rioux John D, Lassen Kara G, Xavier Ramnik |
| Association of common variation in ADD3 and GPC1 with biliary atresia susceptibility. Aging 2020 4 12 (8): 7163-7182. Bai Mei-Rong, Niu Wei-Bo, Zhou Ying, Gong Yi-Ming, Lu Yan-Jiao, Yu Xian-Xian, Wei Zhi-Liang, Wu Wenjie, Song Huan-Lei, Yu Wen-Wen, Gu Bei-Lin, Cai Wei, Chu X |
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