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Cytogenetic aspects of Werner syndrome.
Salk D, Au K, Hoehn H, Martin GM. Salk D, et al. Among authors: martin gm. Adv Exp Med Biol. 1985;190:541-6. doi: 10.1007/978-1-4684-7853-2_27. Adv Exp Med Biol. 1985. PMID: 4083162 No abstract available.
Cellular aging in Werner's syndrome: a unique phenotype?
Norwood TH, Hoehn H, Salk D, Martin GM. Norwood TH, et al. Among authors: martin gm. J Invest Dermatol. 1979 Jul;73(1):92-6. doi: 10.1111/1523-1747.ep12532778. J Invest Dermatol. 1979. PMID: 448183
Homozygosity mapping and Werner's syndrome.
Schellenberg GD, Martin GM, Wijsman EM, Nakura J, Miki T, Ogihara T. Schellenberg GD, et al. Among authors: martin gm. Lancet. 1992 Apr 18;339(8799):1002. doi: 10.1016/0140-6736(92)91590-5. Lancet. 1992. PMID: 1348795 No abstract available.
The Werner syndrome protein is a DNA helicase.
Gray MD, Shen JC, Kamath-Loeb AS, Blank A, Sopher BL, Martin GM, Oshima J, Loeb LA. Gray MD, et al. Among authors: martin gm. Nat Genet. 1997 Sep;17(1):100-3. doi: 10.1038/ng0997-100. Nat Genet. 1997. PMID: 9288107
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. Among authors: martin gm. Science. 1996 Apr 12;272(5259):258-62. doi: 10.1126/science.272.5259.258. Science. 1996. PMID: 8602509
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