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Mapping ESTs by fiber-FISH.
Horelli-Kuitunen N, Aaltonen J, Yaspo ML, Eeva M, Wessman M, Peltonen L, Palotie A. Horelli-Kuitunen N, et al. Among authors: wessman m. Genome Res. 1999 Jan;9(1):62-71. Genome Res. 1999. PMID: 9927485 Free PMC article.
Clinical characteristics of migraine concordant monozygotic twin pairs.
Kallela M, Wessman M, Färkkilä M, Palotie A, Koskenvuo M, Honkasalo ML, Kaprio J. Kallela M, et al. Among authors: wessman m. Acta Neurol Scand. 1999 Oct;100(4):254-9. doi: 10.1111/j.1600-0404.1999.tb00390.x. Acta Neurol Scand. 1999. PMID: 10510686
Fine mapping of Hyplip1 and the human homolog, a potential locus for FCHL.
Pajukanta P, Bodnar JS, Sallinen R, Chu M, Airaksinen T, Xiao Q, Castellani LW, Sheth SS, Wessman M, Palotie A, Sinsheimer JS, Demant P, Lusis AJ, Peltonen L. Pajukanta P, et al. Among authors: wessman m. Mamm Genome. 2001 Mar;12(3):238-45. doi: 10.1007/s003350010265. Mamm Genome. 2001. PMID: 11252174
Physical mapping of mouse collagen genes on chromosome 10 by high-resolution FISH.
Sallinen R, Latvanlehto A, Kvist AP, Rehn M, Eerola I, Chu ML, Bonaldo P, Saitta B, Bressan GM, Pihlajaniemi T, Vuorio E, Palotie A, Wessman M, Horelli-Kuitunen N. Sallinen R, et al. Among authors: wessman m. Mamm Genome. 2001 May;12(5):340-6. doi: 10.1007/s003350010271. Mamm Genome. 2001. PMID: 11331940
Confirmation of the type 2 myotonic dystrophy (CCTG)n expansion mutation in patients with proximal myotonic myopathy/proximal myotonic dystrophy of different European origins: a single shared haplotype indicates an ancestral founder effect.
Bachinski LL, Udd B, Meola G, Sansone V, Bassez G, Eymard B, Thornton CA, Moxley RT, Harper PS, Rogers MT, Jurkat-Rott K, Lehmann-Horn F, Wieser T, Gamez J, Navarro C, Bottani A, Kohler A, Shriver MD, Sallinen R, Wessman M, Zhang S, Wright FA, Krahe R. Bachinski LL, et al. Among authors: wessman m. Am J Hum Genet. 2003 Oct;73(4):835-48. doi: 10.1086/378566. Epub 2003 Sep 10. Am J Hum Genet. 2003. PMID: 12970845 Free PMC article.
155 results