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1954 1
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Page 1
Fibrillin (FBN1) mutations in Marfan syndrome.
Hayward C, Keston M, Brock DJ, Dietz HC. Hayward C, et al. Among authors: keston m. Hum Mutat. 1992;1(1):79. doi: 10.1002/humu.1380010115. Hum Mutat. 1992. PMID: 1301195 No abstract available.
Clonidine in hypertension: a 6-year review.
Lawson AA, Keston M. Lawson AA, et al. Among authors: keston m. Curr Med Res Opin. 1979;6(3):168-74. doi: 10.1185/03007997909109416. Curr Med Res Opin. 1979. PMID: 520022
Flurazepam and meprobamate: a clinical trial.
Keston M, Brocklehurst JC. Keston M, et al. Age Ageing. 1974 Feb;3(1):54-8. doi: 10.1093/ageing/3.1.54. Age Ageing. 1974. PMID: 4597061 Clinical Trial. No abstract available.
Cystic fibrosis patients bearing both the common missense mutation Gly----Asp at codon 551 and the delta F508 mutation are clinically indistinguishable from delta F508 homozygotes, except for decreased risk of meconium ileus.
Hamosh A, King TM, Rosenstein BJ, Corey M, Levison H, Durie P, Tsui LC, McIntosh I, Keston M, Brock DJ, et al. Hamosh A, et al. Among authors: keston m. Am J Hum Genet. 1992 Aug;51(2):245-50. Am J Hum Genet. 1992. PMID: 1379413 Free PMC article.
16 results