Peltonen L - Search Results

1

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: peltonen l. Nat Genet. 1994 Feb;6(2):117-8. doi: 10.1038/ng0294-117. Nat Genet. 1994. PMID: 8162064 No abstract available.

2

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: peltonen l. Hum Genet. 1990 Oct;85(5):541-5. doi: 10.1007/BF00194234. Hum Genet. 1990. PMID: 1977684

3

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: peltonen l. Clin Genet. 1993 Apr;43(4):190-5. doi: 10.1111/j.1399-0004.1993.tb04446.x. Clin Genet. 1993. PMID: 8101149

4

Usefulness of chromosome 19 RFLP haplotypes in the diagnosis of myotonic dystrophy.

Nokelainen PT, Alanen-Kurki L, Somer HV, Pihko SH, Peltonen L. Nokelainen PT, et al. Among authors: peltonen l. Muscle Nerve. 1991 May;14(5):451-6. doi: 10.1002/mus.880140511. Muscle Nerve. 1991. PMID: 1678492

5

The genetic locus for free sialic acid storage disease maps to the long arm of chromosome 6.

Haataja L, Schleutker J, Laine AP, Renlund M, Savontaus ML, Dib C, Weissenbach J, Peltonen L, Aula P. Haataja L, et al. Among authors: peltonen l. Am J Hum Genet. 1994 Jun;54(6):1042-9. Am J Hum Genet. 1994. PMID: 8198127 Free PMC article.

6

Linkage analyses in tibial muscular dystrophy.

Nokelainen P, Udd B, Somer H, Peltonen L. Nokelainen P, et al. Among authors: peltonen l. Hum Hered. 1996 Mar-Apr;46(2):98-107. doi: 10.1159/000154334. Hum Hered. 1996. PMID: 8666419

7

The genetic relationship between the Finns and the Finnish Saami (Lapps): analysis of nuclear DNA and mtDNA.

Lahermo P, Sajantila A, Sistonen P, Lukka M, Aula P, Peltonen L, Savontaus ML. Lahermo P, et al. Among authors: peltonen l. Am J Hum Genet. 1996 Jun;58(6):1309-22. Am J Hum Genet. 1996. PMID: 8651309 Free PMC article.

8

Ancestral differences in the distribution of the delta 2642 glutamic acid polymorphism is associated with varying CAG repeat lengths on normal chromosomes: insights into the genetic evolution of Huntington disease.

Almqvist E, Spence N, Nichol K, Andrew SE, Vesa J, Peltonen L, Anvret M, Goto J, Kanazawa I, Goldberg YP, et al. Almqvist E, et al. Among authors: peltonen l. Hum Mol Genet. 1995 Feb;4(2):207-14. doi: 10.1093/hmg/4.2.207. Hum Mol Genet. 1995. PMID: 7757069

9

A microsatellite polymorphism in the von Willebrand factor gene: comparison of allele frequencies in different population samples and evaluation for forensic medicine.

Sajantila A, Pacek P, Lukka M, Syvänen AC, Nokelainen P, Sistonen P, Peltonen L, Budowle B. Sajantila A, et al. Among authors: peltonen l. Forensic Sci Int. 1994 Sep 16;68(2):91-102. doi: 10.1016/0379-0738(94)90307-7. Forensic Sci Int. 1994. PMID: 7988968

10

Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegia.

Suomalainen A, Majander A, Haltia M, Somer H, Lönnqvist J, Savontaus ML, Peltonen L. Suomalainen A, et al. Among authors: peltonen l. J Clin Invest. 1992 Jul;90(1):61-6. doi: 10.1172/JCI115856. J Clin Invest. 1992. PMID: 1634620 Free PMC article.

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