Johnson K - Search Results

1

Linkage disequilibrium detected between dystrophia myotonica and APOC2 locus in the Finnish population.

Nokelainen P, Alanen-Kurki L, Winqvist R, Falck B, Somer H, Leisti J, Johnson K, Savontaus ML, Peltonen L. Nokelainen P, et al. Among authors: johnson k. Hum Genet. 1990 Oct;85(5):541-5. doi: 10.1007/BF00194234. Hum Genet. 1990. PMID: 1977684

2

The DM mutation; diagnostic applications in the Finnish population.

Nokelainen P, Shelbourne P, Shaw D, Brook JD, Harley HG, Johnson K, Somer H, Savontaus ML, Peltonen L. Nokelainen P, et al. Among authors: johnson k. Clin Genet. 1993 Apr;43(4):190-5. doi: 10.1111/j.1399-0004.1993.tb04446.x. Clin Genet. 1993. PMID: 8101149

3

Recombination events that locate myotonic dystrophy distal to APOC2 on 19q.

Johnson K, Shelbourne P, Davies J, Buxton J, Nimmo E, Anvret M, Bonduelle M, Williamson B, Savontaus ML. Johnson K, et al. Genomics. 1989 Nov;5(4):746-51. doi: 10.1016/0888-7543(89)90116-x. Genomics. 1989. PMID: 2591962

4

Segregation of linked probes to myotonic dystrophy in a family demonstrating that 152 and APOC2 are on the same side of DM on 19q.

Johnson K, Nimmo E, Jones P, Weiss M, Savontaus ML, Anvret M, Bartlett R, Roses A, Shaw D, Harper PS, et al. Johnson K, et al. Hum Genet. 1988 Dec;80(4):379-81. doi: 10.1007/BF00273655. Hum Genet. 1988. PMID: 3198115

5

Unstable DNA may be responsible for the incomplete penetrance of the myotonic dystrophy phenotype.

Shelbourne P, Winqvist R, Kunert E, Davies J, Leisti J, Thiele H, Bachmann H, Buxton J, Williamson B, Johnson K. Shelbourne P, et al. Among authors: johnson k. Hum Mol Genet. 1992 Oct;1(7):467-73. doi: 10.1093/hmg/1.7.467. Hum Mol Genet. 1992. PMID: 1307246

6

Meiotic drive at the myotonic dystrophy locus?

Carey N, Johnson K, Nokelainen P, Peltonen L, Savontaus ML, Juvonen V, Anvret M, Grandell U, Chotai K, Robertson E, et al. Carey N, et al. Among authors: johnson k. Nat Genet. 1994 Feb;6(2):117-8. doi: 10.1038/ng0294-117. Nat Genet. 1994. PMID: 8162064 No abstract available.

7

A new polymorphic probe which defines the region of chromosome 19 containing the myotonic dystrophy locus.

Johnson K, Shelbourne P, Davies J, Buxton J, Nimmo E, Siciliano MJ, Bachinski LL, Anvret M, Harley H, Rundle S, et al. Johnson K, et al. Am J Hum Genet. 1990 Jun;46(6):1073-81. Am J Hum Genet. 1990. PMID: 1971149 Free PMC article.

8

Comparison of the myotonic dystrophy associated CTG repeat in European and Japanese populations.

Davies J, Yamagata H, Shelbourne P, Buxton J, Ogihara T, Nokelainen P, Nakagawa M, Williamson R, Johnson K, Miki T. Davies J, et al. Among authors: johnson k. J Med Genet. 1992 Nov;29(11):766-9. doi: 10.1136/jmg.29.11.766. J Med Genet. 1992. PMID: 1453423 Free PMC article.

9

D19S51 is closely linked with and maps distal to the myotonic dystrophy locus on 19q.

Tsilfidis C, MacKenzie AE, Shutler G, Leblond S, Bailly J, Johnson K, Williamson R, Siegel-Bartelt J, Korneluk RG, Shelbourne P. Tsilfidis C, et al. Among authors: johnson k. Am J Hum Genet. 1991 Nov;49(5):961-5. Am J Hum Genet. 1991. PMID: 1928101 Free PMC article.

10

Confirmation and refinement of the localisation of the c-MEL locus on chromosome 19 by physical and genetic mapping.

Nimmo E, Padua RA, Hughes D, Brook JD, Williamson R, Johnson KJ. Nimmo E, et al. Among authors: johnson kj. Hum Genet. 1989 Mar;81(4):382-4. doi: 10.1007/BF00283697. Hum Genet. 1989. PMID: 2564840

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