HuGE Literature Finder
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Genomic analysis of childhood hearing loss in the Yoruba population of Nigeria. European journal of human genetics : EJHG 2021 Nov . Adeyemo Adebolajo, Faridi Rabia, Chattaraj Parna, Yousaf Rizwan, Tona Risa, Okorie Samuel, Bharadwaj Thashi, Nouel-Saied Liz M, Acharya Anushree, Schrauwen Isabelle, Morell Robert J, Leal Suzanne M, Friedman Thomas B, Griffith Andrew J, Roux Isabel |
Variants in WFS1 and Other Mendelian Deafness Genes Are Associated with Cisplatin-Associated Ototoxicity.
![]() Clinical cancer research : an official journal of the American Association for Cancer Research 2016 Dec . Wheeler Heather E, Gamazon Eric R, Frisina Robert, Perez-Cervantes Carlos, El Charif Omar, Mapes Brandon, Fossa Sophie D, Feldman Darren, Hamilton Robert, Vaughn David J, Beard Clair, Fung Chunkit, Kollmannsberger Christian, Kim Jeri, Mushiroda Taisei, Kubo Michiaki, Ardeshir-Rouhani-Fard Shirin, Einhorn Lawrence H, Cox Nancy, Dolan M Eileen, Travis Lo |
Targeted genomic capture and massively parallel sequencing to identify novel variants causing Chinese hereditary hearing loss. Journal of translational medicine 2014 12 (1): 311. Wei Qinjun, Zhu Hongmei, Qian Xuli, Chen Zhibin, Yao Jun, Lu Yajie, Cao Xin, Xing Guangqi |
Testing of diabetes-associated WFS1 polymorphisms in the Diabetes Prevention Program. Diabetologia 2008 Mar 51 (3): 451-7. Florez J C, Jablonski K A, McAteer J, Sandhu M S, Wareham N J, Barroso I, Franks P W, Altshuler D, Knowler W C, |
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