Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Biliary Atresia and NOTCH2[original query] |
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Combined genetic analyses can achieve efficient diagnostic yields for subjects with Alagille syndrome and incomplete Alagille syndrome. Acta paediatrica (Oslo, Norway : 1992) 2017 Jul . Ohashi Kei, Togawa Takao, Sugiura Tokio, Ito Koichi, Endo Takeshi, Aoyama Kohei, Negishi Yutaka, Kudo Toyoichiro, Ito Reiko, Saitoh Shin |
Epistatic Association of CD14 and NOTCH2 Genetic Polymorphisms with Biliary Atresia in a Southern Chinese Population. Molecular therapy. Nucleic acids 2018 Oct 13 590-595. Lin Zefeng, Xie Xiaoli, Lin Huiting, Fu Ming, Su Liang, Tong Yanlu, Chen Hongjiao, Wang Hezhen, Zhao Jinglu, Xia Huimin, Zhang Yan, Zhang Ruizho |
Exome-wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child-parent trios and a case-control design to identify novel rare variants. American journal of medical genetics. Part A 2023 3 . Sok Pagna, Sabo Aniko, Almli Lynn M, Jenkins Mary M, Nembhard Wendy N, Agopian A J, Bamshad Michael J, Blue Elizabeth E, Brody Lawrence C, Brown Austin L, Browne Marilyn L, Canfield Mark A, Carmichael Suzan L, Chong Jessica X, Dugan-Perez Shannon, Feldkamp Marcia L, Finnell Richard H, Gibbs Richard A, Kay Denise M, Lei Yunping, Meng Qingchang, Moore Cynthia A, Mullikin James C, Muzny Donna, Olshan Andrew F, Pangilinan Faith, Reefhuis Jennita, Romitti Paul A, Schraw Jeremy M, Shaw Gary M, Werler Martha M, Harpavat Sanjiv, Lupo Philip J, |
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