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Journal Abstract Search
101 related items for PubMed ID: 9752308
1. [The gene of Gorlin's syndrome (basocellular nevomatosis) and the revival of the developmental genes in human carcinogenesis]. Molès JP. Bull Cancer; 1998 Mar; 85(3):207-8. PubMed ID: 9752308 [Abstract] [Full Text] [Related]
18. Identification of mutations in the human PATCHED gene in sporadic basal cell carcinomas and in patients with the basal cell nevus syndrome. Aszterbaum M, Rothman A, Johnson RL, Fisher M, Xie J, Bonifas JM, Zhang X, Scott MP, Epstein EH. J Invest Dermatol; 1998 Jun 11; 110(6):885-8. PubMed ID: 9620294 [Abstract] [Full Text] [Related]
19. A novel missense mutation in the PTCH1 gene in a premature case of nevoid basal cell carcinoma syndrome. Nakamura M, Tokura Y. Eur J Dermatol; 2009 Jun 11; 19(3):262-3. PubMed ID: 19213655 [No Abstract] [Full Text] [Related]
20. Mutation in exon 7 of PTCH deregulates SHH/PTCH/SMO signaling: possible linkage to WNT. Musani V, Gorry P, Basta-Juzbasic A, Stipic T, Miklic P, Levanat S. Int J Mol Med; 2006 May 11; 17(5):755-9. PubMed ID: 16596257 [Abstract] [Full Text] [Related] Page: [Next] [New Search]