Palotie A - Search Results

1

Polymorphic restriction sites of type II collagen gene: their location and frequencies in the Finnish population.

Väisänen P, Elima K, Palotie A, Peltonen L, Vuorio E. Väisänen P, et al. Among authors: palotie a. Hum Hered. 1988;38(2):65-71. doi: 10.1159/000153760. Hum Hered. 1988. PMID: 2897945

2

RFLP analysis of three different types of acute intermittent porphyria.

Kauppinen R, Peltonen L, Palotie A, Mustajoki P. Kauppinen R, et al. Among authors: palotie a. Hum Genet. 1990 Jul;85(2):160-4. doi: 10.1007/BF00193189. Hum Genet. 1990. PMID: 1973403

3

Predisposition to familial osteoarthrosis linked to type II collagen gene.

Palotie A, Väisänen P, Ott J, Ryhänen L, Elima K, Vikkula M, Cheah K, Vuorio E, Peltonen L. Palotie A, et al. Lancet. 1989 Apr 29;1(8644):924-7. doi: 10.1016/s0140-6736(89)92507-5. Lancet. 1989. PMID: 2565419

4

Multiallelic polymorphism of the cartilage collagen gene: no association with osteoarthrosis.

Vikkula M, Nissilä M, Hirvensalo E, Nuotio P, Palotie A, Aho K, Peltonen L. Vikkula M, et al. Among authors: palotie a. Ann Rheum Dis. 1993 Oct;52(10):762-4. doi: 10.1136/ard.52.10.762. Ann Rheum Dis. 1993. PMID: 8257213 Free PMC article.

5

Assignment of the locus for a new lethal neonatal metabolic syndrome to 2q33-37.

Visapää I, Fellman V, Varilo T, Palotie A, Raivio KO, Peltonen L. Visapää I, et al. Among authors: palotie a. Am J Hum Genet. 1998 Nov;63(5):1396-403. doi: 10.1086/302123. Am J Hum Genet. 1998. PMID: 9792866 Free PMC article.

6

Association of FXIII Val34Leu with decreased risk of myocardial infarction in Finnish males.

Wartiovaara U, Perola M, Mikkola H, Tötterman K, Savolainen V, Penttilä A, Grant PJ, Tikkanen MJ, Vartiainen E, Karhunen PJ, Peltonen L, Palotie A. Wartiovaara U, et al. Among authors: palotie a. Atherosclerosis. 1999 Feb;142(2):295-300. doi: 10.1016/s0021-9150(98)00241-x. Atherosclerosis. 1999. PMID: 10030380

7

Assignment of a novel locus for autosomal recessive congenital ichthyosis to chromosome 19p13.1-p13.2.

Virolainen E, Wessman M, Hovatta I, Niemi KM, Ignatius J, Kere J, Peltonen L, Palotie A. Virolainen E, et al. Among authors: palotie a. Am J Hum Genet. 2000 Mar;66(3):1132-7. doi: 10.1086/302813. Am J Hum Genet. 2000. PMID: 10712223 Free PMC article.

8

Exclusion map of Salla disease: attempts to localize the disease gene using a computer program.

Haataja L, Schleutker J, Renlund M, Palotie A, Peltonen L, Aula P. Haataja L, et al. Among authors: palotie a. Hum Genet. 1992 Jan;88(3):298-300. doi: 10.1007/BF00197263. Hum Genet. 1992. PMID: 1733832

9

Huntington disease in Finland: linkage disequilibrium of chromosome 4 RFLP haplotypes and exclusion of a tight linkage between the disease and D4S43 locus.

Ikonen E, Palo J, Ott J, Gusella J, Somer H, Karila L, Palotie A, Peltonen L. Ikonen E, et al. Among authors: palotie a. Am J Hum Genet. 1990 Jan;46(1):5-11. Am J Hum Genet. 1990. PMID: 1967208 Free PMC article.

10

Marfan syndrome: exclusion of genetic linkage to five genes coding for connective tissue components in the long arm of chromosome 2.

Kainulainen K, Savolainen A, Palotie A, Kaitila I, Rosenbloom J, Peltonen L. Kainulainen K, et al. Among authors: palotie a. Hum Genet. 1990 Feb;84(3):233-6. doi: 10.1007/BF00200565. Hum Genet. 1990. PMID: 1968032

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