Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Syndrome and CELSR3[original query] |
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De Novo Coding Variants Are Strongly Associated with Tourette Disorder. Neuron 2017 May 94 (3): 486-499.e9. Willsey A Jeremy, Fernandez Thomas V, Yu Dongmei, King Robert A, Dietrich Andrea, Xing Jinchuan, Sanders Stephan J, Mandell Jeffrey D, Huang Alden Y, Richer Petra, Smith Louw, Dong Shan, Samocha Kaitlin E, , , Neale Benjamin M, Coppola Giovanni, Mathews Carol A, Tischfield Jay A, Scharf Jeremiah M, State Matthew W, Heiman Gary |
CELSR1 Risk Alleles in Familial Bicuspid Aortic Valve and Hypoplastic Left Heart Syndrome. Circulation. Genomic and precision medicine 2022 2 15 (2): e003523. Theis Jeanne L, Niaz Talha, Sundsbak Rhianna S, Fogarty Zachary C, Bamlet William R, Hagler Donald J, Olson Timothy |
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- Page last updated:May 06, 2024
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