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Mutations of the human PTEN gene.
Bonneau D, Longy M. Bonneau D, et al. Among authors: longy m. Hum Mutat. 2000;16(2):109-22. doi: 10.1002/1098-1004(200008)16:2<109::AID-HUMU3>3.0.CO;2-0. Hum Mutat. 2000. PMID: 10923032 Review.
Allelic imbalance, including deletion of PTEN/MMACI, at the Cowden disease locus on 10q22-23, in hamartomas from patients with Cowden syndrome and germline PTEN mutation.
Marsh DJ, Dahia PL, Coulon V, Zheng Z, Dorion-Bonnet F, Call KM, Little R, Lin AY, Eeles RA, Goldstein AM, Hodgson SV, Richardson AL, Robinson BG, Weber HC, Longy M, Eng C. Marsh DJ, et al. Among authors: longy m. Genes Chromosomes Cancer. 1998 Jan;21(1):61-9. doi: 10.1002/(sici)1098-2264(199801)21:1<61::aid-gcc8>3.0.co;2-6. Genes Chromosomes Cancer. 1998. PMID: 9443042
PTEN/MMAC1/TEP1 involvement in primary prostate cancers.
Pesche S, Latil A, Muzeau F, Cussenot O, Fournier G, Longy M, Eng C, Lidereau R. Pesche S, et al. Among authors: longy m. Oncogene. 1998 Jun 4;16(22):2879-83. doi: 10.1038/sj.onc.1202081. Oncogene. 1998. PMID: 9671408
Spectrum of PTCH1 mutations in French patients with Gorlin syndrome.
Boutet N, Bignon YJ, Drouin-Garraud V, Sarda P, Longy M, Lacombe D, Gorry P. Boutet N, et al. Among authors: longy m. J Invest Dermatol. 2003 Sep;121(3):478-81. doi: 10.1046/j.1523-1747.2003.12423.x. J Invest Dermatol. 2003. PMID: 12925203 Free article.
[Cowden's disease in an adolescent].
Mcheik JN, Vabres P, Bonneau D, Longy M, Levard G. Mcheik JN, et al. Among authors: longy m. Ann Chir. 2002 Feb;127(2):138-41. doi: 10.1016/s0003-3944(01)00690-3. Ann Chir. 2002. PMID: 11885374 French.
203 results