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Query Trace: Syndrome and FCRL3[original query]

From Genetic Predisposition to Molecular Mechanisms of Autoimmune Primary Adrenal Insufficiency. Frontiers of hormone research 2016 46 115-32. Falorni Alberto, Brozzetti Annalisa, Perniola Rober Similar articles in PubMed
MHC2TA and FCRL3 genes are not associated with rheumatoid arthritis in Mexican patients. Rheumatology international 2015 Sep . Mendoza Rincón J F, Rodríguez Elias A K, Fragoso J M, Vargas Alarcón G, Maldonado Murillo K, Rivas Jiménez M L, Barbosa Cobos R E, Jimenez Morales S, Lugo Zamudio G, Tovilla Zárate C, Ramírez Bello Similar articles in PubMed
Fc receptor like 3 in Chinese patients of Han nationality with Guillain-Barré syndrome. Journal of neuroimmunology 2012 Mar . Sang D, Chen Q, Liu X, Qu H, Wei D, Yin L, Zhang L Similar articles in PubMed
Polymorphisms of FCRL3 in a Chinese population with Vogt-Koyanagi-Harada (VKH) syndrome. Molecular vision 2009 15 955-61. Li Ke, Yang Peizeng, Zhao Min, Hou Shengping, Du Liping, Zhou Hongyan, Kijlstra Ai Similar articles in PubMed