Peltonen L - Search Results

1

Lethal congenital contracture syndrome (LCCS), a fetal anterior horn cell disease, is not linked to the SMA 5q locus.

Vuopala K, Mäkelä-Bengs P, Suomalainen A, Herva R, Leisti J, Peltonen L. Vuopala K, et al. Among authors: peltonen l. J Med Genet. 1995 Jan;32(1):36-8. doi: 10.1136/jmg.32.1.36. J Med Genet. 1995. PMID: 7897624 Free PMC article.

2

Assignment of the disease locus for lethal congenital contracture syndrome to a restricted region of chromosome 9q34, by genome scan using five affected individuals.

Mäkelä-Bengs P, Järvinen N, Vuopala K, Suomalainen A, Ignatius J, Sipilä M, Herva R, Palotie A, Peltonen L. Mäkelä-Bengs P, et al. Among authors: peltonen l. Am J Hum Genet. 1998 Aug;63(2):506-16. doi: 10.1086/301968. Am J Hum Genet. 1998. PMID: 9683599 Free PMC article.

3

Random search for shared chromosomal regions in four affected individuals: the assignment of a new hereditary ataxia locus.

Nikali K, Suomalainen A, Terwilliger J, Koskinen T, Weissenbach J, Peltonen L. Nikali K, et al. Among authors: peltonen l. Am J Hum Genet. 1995 May;56(5):1088-95. Am J Hum Genet. 1995. PMID: 7726163 Free PMC article.

4

An autosomal locus predisposing to multiple deletions of mtDNA on chromosome 3p.

Kaukonen JA, Amati P, Suomalainen A, Rötig A, Piscaglia MG, Salvi F, Weissenbach J, Fratta G, Comi G, Peltonen L, Zeviani M. Kaukonen JA, et al. Among authors: peltonen l. Am J Hum Genet. 1996 Apr;58(4):763-9. Am J Hum Genet. 1996. PMID: 8644740 Free PMC article.

5

Improved prenatal diagnosis of the congenital nephrotic syndrome of the Finnish type based on DNA analysis.

Männikkö M, Kestilä M, Lenkkeri U, Alakurtti H, Holmberg C, Leisti J, Salonen R, Aula P, Mustonen A, Peltonen L, Tryggvason K. Männikkö M, et al. Among authors: peltonen l. Kidney Int. 1997 Mar;51(3):868-72. doi: 10.1038/ki.1997.122. Kidney Int. 1997. PMID: 9067923 Free article.

6

Assignment of the tibial muscular dystrophy locus to chromosome 2q31.

Haravuori H, Mäkelä-Bengs P, Udd B, Partanen J, Pulkkinen L, Somer H, Peltonen L. Haravuori H, et al. Among authors: peltonen l. Am J Hum Genet. 1998 Mar;62(3):620-6. doi: 10.1086/301752. Am J Hum Genet. 1998. PMID: 9497249 Free PMC article.

7

LCCS: a lethal motoneuron disease of the fetus maps to chromosome 9q34.

Järvinen N, Mäkelä-Bengs P, Suomalainen A, Vuopala K, Herva R, Palotie A, Peltonen L. Järvinen N, et al. Among authors: peltonen l. Ann N Y Acad Sci. 1998 Oct 23;857:260-2. doi: 10.1111/j.1749-6632.1998.tb10127.x. Ann N Y Acad Sci. 1998. PMID: 9917852 No abstract available.

8

Tracing an ancestral mutation: genealogical and haplotype analysis of the infantile onset spinocerebellar ataxia locus.

Varilo T, Nikali K, Suomalainen A, Lönnqvist T, Peltonen L. Varilo T, et al. Among authors: peltonen l. Genome Res. 1996 Sep;6(9):870-5. doi: 10.1101/gr.6.9.870. Genome Res. 1996. PMID: 8889554 Free article.

9

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

10

An autosomal locus predisposing to deletions of mitochondrial DNA.

Suomalainen A, Kaukonen J, Amati P, Timonen R, Haltia M, Weissenbach J, Zeviani M, Somer H, Peltonen L. Suomalainen A, et al. Among authors: peltonen l. Nat Genet. 1995 Feb;9(2):146-51. doi: 10.1038/ng0295-146. Nat Genet. 1995. PMID: 7719341

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

990 results

Search Page

Filters