Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Syndrome and FGF3[original query] |
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Genome-wide copy number variation analysis of a Branchio-oto-renal syndrome cohort identifies a recombination hotspot and implicates new candidate genes. Human genetics 2013 Dec 132 (12): 1339-50. Brophy Patrick D, Alasti Fatemeh, Darbro Benjamin W, Clarke Jason, Nishimura Carla, Cobb Bryan, Smith Richard J, Manak J Robe |
Evidence of genetic variations associated with rotator cuff disease. Journal of shoulder and elbow surgery / American Shoulder and Elbow Surgeons ... [et al.] 2014 Feb 23 (2): 227-35. Motta Geraldo da Rocha, Amaral Marcus Vinícius, Rezende Eduardo, Pitta Rafael, Vieira Thays Cristine dos Santos, Duarte Maria Eugenia Leite, Vieira Alexandre Rezende, Casado Priscila Ladei |
De novo 11q13.3q13.4 deletion in a patient with Fanconi renotubular syndrome and intellectual disability: Case report and review of literature. Frontiers in pediatrics 2023 5 11 1097062. Yingxiao Shen, Xiaoqin Xu, Jiansong Chen, Jingjing Wang, Guanping Dong, Ke Huang, Junfen Fu, Dingwen Wu, Wei |
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- Page last updated:Apr 16, 2024
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