Human Genome Epidemiology Literature Finder
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Records 1 - 4 (of 4 Records) |
| Query Trace: Disease and UFD1L[original query] |
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| A family- and population-based study of the UFD1L gene for schizophrenia. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008 Oct 147B (7): 1076-9. Xie Lin, Ye Lin, Ju Guizhi, Xu Qi, Zhang Xuan, Liu Shuzheng, Shi Jieping, Yu Yaqin, Wang Zhenqi, Shen Yan, Wei J |
| Mitochondrial Citrate Transporter-dependent Metabolic Signature in the 22q11.2 Deletion Syndrome. The Journal of biological chemistry 2015 Sep 290 (38): 23240-53. Napoli Eleonora, Tassone Flora, Wong Sarah, Angkustsiri Kathleen, Simon Tony J, Song Gyu, Giulivi Cecil |
| Genetic Bases of Bicuspid Aortic Valve: The Contribution of Traditional and High-Throughput Sequencing Approaches on Research and Diagnosis. Frontiers in physiology 2017 8 612. Giusti Betti, Sticchi Elena, De Cario Rosina, Magi Alberto, Nistri Stefano, Pepe Guglielmi |
| Size matters: Large copy number losses in Hirschsprung disease patients reveal genes involved in enteric nervous system development. PLoS genetics 2021 8 17 (8): e1009698. Kuil Laura E, MacKenzie Katherine C, Tang Clara S, Windster Jonathan D, Le Thuy Linh, Karim Anwarul, de Graaf Bianca M, van der Helm Robert, van Bever Yolande, Sloots Cornelius E J, Meeussen Conny, Tibboel Dick, de Klein Annelies, Wijnen René M H, Amiel Jeanne, Lyonnet Stanislas, Garcia-Barcelo Maria-Mercè, Tam Paul K H, Alves Maria M, Brooks Alice S, Hofstra Robert M W, Brosens Erw |
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