Keston M[au] - Search Results

Year	Number of Results
1954	1
1955	1
1974	1
1979	1
1987	1
1988	2
1989	1
1990	1
1991	3
1992	4
2024	0

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.

2

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

3

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.

4

Marfan syndrome: no evidence for heterogeneity in different populations, and more precise mapping of the gene.

Kainulainen K, Steinmann B, Collins F, Dietz HC, Francomano CA, Child A, Kilpatrick MW, Brock DJ, Keston M, Pyeritz RE, et al. Kainulainen K, et al. Among authors: keston m. Am J Hum Genet. 1991 Sep;49(3):662-7. Am J Hum Genet. 1991. PMID: 1882844 Free PMC article.

5

Exclusion of the alpha 2(I) and alpha 1(III) collagen genes as the mutant loci in a Marfan syndrome family.

Dalgleish R, Hawkins JR, Keston M. Dalgleish R, et al. Among authors: keston m. J Med Genet. 1987 Mar;24(3):148-51. doi: 10.1136/jmg.24.3.148. J Med Genet. 1987. PMID: 2883320 Free PMC article.

6

A cytogenetic study of 47,XXY males of known origin and their parents.

Jacobs PA, Bacino C, Hassold T, Morton NE, Keston M, Lee M. Jacobs PA, et al. Among authors: keston m. Ann Hum Genet. 1988 Oct;52(4):319-25. doi: 10.1111/j.1469-1809.1988.tb01111.x. Ann Hum Genet. 1988. PMID: 3268043

7

Three novel mutations in the cystic fibrosis gene detected by chemical cleavage: analysis of variant splicing and a nonsense mutation.

Jones CT, McIntosh I, Keston M, Ferguson A, Brock DJ. Jones CT, et al. Among authors: keston m. Hum Mol Genet. 1992 Apr;1(1):11-7. doi: 10.1093/hmg/1.1.11. Hum Mol Genet. 1992. PMID: 1284466

8

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.

9

An implantable device for long term venous access in chronic lung conditions.

Davies MJ, Wilson RG, Keston M, Nixon SJ. Davies MJ, et al. Among authors: keston m. BMJ. 1991 Mar 9;302(6776):570-1. doi: 10.1136/bmj.302.6776.570. BMJ. 1991. PMID: 2021722 Free PMC article. No abstract available.

10

Klinefelter's syndrome: an analysis of the origin of the additional sex chromosome using molecular probes.

Jacobs PA, Hassold TJ, Whittington E, Butler G, Collyer S, Keston M, Lee M. Jacobs PA, et al. Among authors: keston m. Ann Hum Genet. 1988 May;52(2):93-109. doi: 10.1111/j.1469-1809.1988.tb01084.x. Ann Hum Genet. 1988. PMID: 2907853

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