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

3

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: savontaus ml. Am J Hum Genet. 1996 Jun;58(6):1309-22. Am J Hum Genet. 1996. PMID: 8651309 Free PMC article.

4

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. Among authors: savontaus ml. Genomics. 1989 Nov;5(4):746-51. doi: 10.1016/0888-7543(89)90116-x. Genomics. 1989. PMID: 2591962

5

Gene deletions in X-linked muscular dystrophy.

Lindlöf M, Kiuru A, Kääriäinen H, Kalimo H, Lang H, Pihko H, Rapola J, Somer H, Somer M, Savontaus ML, et al. Lindlöf M, et al. Among authors: savontaus ml. Am J Hum Genet. 1989 Apr;44(4):496-503. Am J Hum Genet. 1989. PMID: 2929594 Free PMC article.

6

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. Among authors: savontaus ml. Hum Genet. 1988 Dec;80(4):379-81. doi: 10.1007/BF00273655. Hum Genet. 1988. PMID: 3198115

7

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: savontaus ml. Am J Hum Genet. 1994 Jun;54(6):1042-9. Am J Hum Genet. 1994. PMID: 8198127 Free PMC article.

8

DNA analysis in Finnish patients with hereditary neuropathy with liability to pressure palsies (HNPP).

Silander K, Halonen P, Sara R, Kalimo H, Falck B, Savontaus ML. Silander K, et al. Among authors: savontaus ml. J Neurol Neurosurg Psychiatry. 1994 Oct;57(10):1260-2. doi: 10.1136/jnnp.57.10.1260. J Neurol Neurosurg Psychiatry. 1994. PMID: 7931393 Free PMC article.

9

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

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: savontaus ml. 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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