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12. Gene symbol: hMSH. Disease: Hereditary nonpolyposis colorectal cancer. Sun MH; Cai Q; Fu G; Ren S; Mo S; Xu Y; Ding C; Zhang T; Zhu X; Xu X; Min D; Cai S; Luo D; Shi Y; Shi D Hum Genet; 2004 Mar; 114(4):409. PubMed ID: 15046092 [No Abstract] [Full Text] [Related]
13. Novel germline hMSH2 genomic deletion and somatic hMSH2 mutations in a hereditary nonpolyposis colorectal cancer family. Miyaki M; Iijima T; Yamaguchi T; Shirahama S; Ito T; Yasuno M; Mori T Mutat Res; 2004 Apr; 548(1-2):19-25. PubMed ID: 15063132 [TBL] [Abstract][Full Text] [Related]
15. New mutation in the hMSH2 gene in a Spanish Muir-Torre syndrome. Caldés T; Godino J; Perez-Segura P; de la Hoya M; Diaz-Rubio E; Benito M Am J Gastroenterol; 2000 Sep; 95(9):2389-90. PubMed ID: 11007253 [No Abstract] [Full Text] [Related]
16. MSH2 genomic deletions are a frequent cause of HNPCC. Wijnen J; van der Klift H; Vasen H; Khan PM; Menko F; Tops C; Meijers Heijboer H; Lindhout D; Møller P; Fodde R Nat Genet; 1998 Dec; 20(4):326-8. PubMed ID: 9843200 [No Abstract] [Full Text] [Related]
18. Identification of a one-base germline deletion (codon 888 del C) and an intron splice acceptor site polymorphism in hMSH2. Swensen J; Lewis CM; Cannon-Albright LA Hum Mutat; 1997; 10(1):80-1. PubMed ID: 9222765 [No Abstract] [Full Text] [Related]
20. A novel missense germline mutation in exon 2 of the hMSH2 gene in a HNPCC family from Southern Italy. Baudi F; Fersini G; Lavecchia A; Terracciano R; Leone F; Quaresima B; Faniello MC; De Paola L; Doldo P; Cuda G; Costanzo F; Venuta S Cancer Lett; 2005 Jun; 223(2):285-91. PubMed ID: 15896463 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]