1) 長谷川匡:ホルマリン固定パラフィン包埋標本から遺伝子変異/発現はどこまで検索できるか? 病理組織検体を用いたFISH検査の有効性と問題点.病理と臨床 24:69-76, 2006
2) 戸口田淳也,中山富貴,長山聡:遺伝子診断-分子生物学的アプローチ.NEWMOOK整形外科 骨・軟部腫瘍(越智隆弘,菊地臣一編),金原出版,pp69-80, 2005
3) http://www.vysis.com
4) Patel RM, Downs-Kelly E, Weiss SW, et al:Dual-color, break-apart fluorescence in situ hybridization for EWS gene rearrangement distinguishes clear cell sarcoma of soft tissue from malignant melanoma. Mod Pathol 18:1585-1590, 2005
5) Yamaguchi U, Hasegawa T, Morimoto Y, et al:A practical approach to clinical diagnosis of Ewing's sarcoma/primitive neuroectodermal tumour and other small round cell tumours sharing EWS rearrangement using new fluorescence in situ hybridization probes for EWSR1 on formalin fixed, paraffin wax embedded tissue. J Clin Pathol 58:1051-1056, 2005
6) Bridge RS, Rajaram V, Dehner LP, et al:Molecular diagnosis of Ewing sarcoma/primitive neuroectodermal tumor in routinely processed tissue:a comparison of two FISH strategies and RT-PCR in malignant round cell tumors. Mod Pathol 19:1-8, 2006
7) Terry J, Barry TS, Horsman DE, et al:Fluorescence in situ hybridization for the detection of t (X;18)(p11.2;q11.2) in a synovial sarcoma tissue microarray using a breakapart-style probe. Diagn Mol Pathol 14:77-82, 2005