Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Syndrome and HPS5[original query] |
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Genome-wide association study identifies two novel regions at 11p15.5-p13 and 1p31 with major impact on acute-phase serum amyloid A.
PLoS genetics 2010 Nov 6 (11): e1001213. Marzi Carola, Albrecht Eva, Hysi Pirro G, Lagou Vasiliki, Waldenberger Melanie, Tönjes Anke, Prokopenko Inga, Heim Katharina, Blackburn Hannah, Ried Janina S, Kleber Marcus E, Mangino Massimo, Thorand Barbara, Peters Annette, Hammond Christopher J, Grallert Harald, Boehm Bernhard O, Kovacs Peter, Geistlinger Ludwig, Prokisch Holger, Winkelmann Bernhard R, Spector Tim D, Wichmann H-Erich, Stumvoll Michael, Soranzo Nicole, März Winfried, Koenig Wolfgang, Illig Thomas, Gieger Christi |
NGS-based 100-gene panel of hypopigmentation identifies mutations in Chinese Hermansky-Pudlak syndrome patients. Pigment cell & melanoma research 2016 Sep . Wei Aihua, Yuan Yefeng, Bai Dayong, Ma Jing, Hao Zhenhua, Zhang Yingzi, Yu Jiaying, Zhou Zhiyong, Yang Lin, Yang Xiumin, Li Li, Li W |
Instability of BLOC-2 and BLOC-3 in Chinese patients with Hermansky-Pudlak syndrome. Pigment cell & melanoma research 2018 11 32 (3): 373-380. Wei Aihua, Yuan Yefeng, Qi Zhan, Liu Teng, Bai Dayong, Zhang Yingzi, Yu Jiaying, Yang Lin, Yang Xiumin, Li W |
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- Page last updated:Apr 22, 2024
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