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Similar articles for PMID: 9048918

84 results

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Page 1
Mutation and haplotype analyses of the Werner's syndrome gene based on its genomic structure: genetic epidemiology in the Japanese population.
Matsumoto T, Imamura O, Yamabe Y, Kuromitsu J, Tokutake Y, Shimamoto A, Suzuki N, Satoh M, Kitao S, Ichikawa K, Kataoka H, Sugawara K, Thomas W, Mason B, Tsuchihashi Z, Drayna D, Sugawara M, Sugimoto M, Furuichi Y, Goto M. Matsumoto T, et al. Hum Genet. 1997 Jul;100(1):123-30. doi: 10.1007/s004390050477. Hum Genet. 1997. PMID: 9225981
LMNA mutations in atypical Werner's syndrome.
Chen L, Lee L, Kudlow BA, Dos Santos HG, Sletvold O, Shafeghati Y, Botha EG, Garg A, Hanson NB, Martin GM, Mian IS, Kennedy BK, Oshima J. Chen L, et al. Lancet. 2003 Aug 9;362(9382):440-5. doi: 10.1016/S0140-6736(03)14069-X. Lancet. 2003. PMID: 12927431
The 1396del A mutation and a missense mutation or a rare polymorphism of the WRN gene detected in a French Werner family with a severe phenotype and a case of an unusual vulvar cancer. Mutations in brief no. 136. Online.
Vidal V, Bay JO, Champomier F, Grancho M, Beauville L, Glowaczower C, Lemery D, Ferrara M, Bignon YJ. Vidal V, et al. Hum Mutat. 1998;11(5):413-4. doi: 10.1002/(SICI)1098-1004(1998)11:5<413::AID-HUMU16>3.0.CO;2-I. Hum Mutat. 1998. PMID: 10206685
Genetic analyses of two cases of Werner's syndrome.
Sogabe Y, Yasuda M, Yokoyama Y, Tamura A, Negishi I, Ohnishi K, Shinozaki T, Ishikawa O. Sogabe Y, et al. Eur J Dermatol. 2004 Nov-Dec;14(6):379-82. Eur J Dermatol. 2004. PMID: 15564200
Positional cloning of the Werner's syndrome gene.
Yu CE, Oshima J, Fu YH, Wijsman EM, Hisama F, Alisch R, Matthews S, Nakura J, Miki T, Ouais S, Martin GM, Mulligan J, Schellenberg GD. Yu CE, et al. Science. 1996 Apr 12;272(5259):258-62. doi: 10.1126/science.272.5259.258. Science. 1996. PMID: 8602509
WRN mutations in Werner syndrome.
Moser MJ, Oshima J, Monnat RJ Jr. Moser MJ, et al. Hum Mutat. 1999;13(4):271-9. doi: 10.1002/(SICI)1098-1004(1999)13:4<271::AID-HUMU2>3.0.CO;2-Q. Hum Mutat. 1999. PMID: 10220139 Review.
A novel mutation in a patient with Werner's syndrome.
Nakayama T, Ochiai T, Takahashi Y, Ohkubo K, Hironaga T, Kokubun S. Nakayama T, et al. Gerontology. 2002 Jul-Aug;48(4):215-9. doi: 10.1159/000058353. Gerontology. 2002. PMID: 12053110
84 results