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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: kiuru a. Am J Hum Genet. 1989 Apr;44(4):496-503. Am J Hum Genet. 1989. PMID: 2929594 Free PMC article.
[Facioscapulohumeral muscular dystrophy].
Halonen P, Alanen A, Falck B, Kalimo H, Kiuru A, Lang H, Savontaus ML, Sonninen V. Halonen P, et al. Among authors: kiuru a. Duodecim. 1990;106(17):1210-8. Duodecim. 1990. PMID: 1670542 Review. Finnish. No abstract available.
The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion.
Koenig M, Beggs AH, Moyer M, Scherpf S, Heindrich K, Bettecken T, Meng G, Müller CR, Lindlöf M, Kaariainen H, de la Chapellet A, Kiuru A, Savontaus ML, Gilgenkrantz H, Récan D, Chelly J, Kaplan JC, Covone AE, Archidiacono N, Romeo G, Liechti-Gailati S, Schneider V, Braga S, Moser H, Darras BT, Murphy P, Francke U, Chen JD, Morgan G, Denton M, Greenberg CR, Wrogemann K, Blonden LA, van Paassen MB, van Ommen GJ, Kunkel LM. Koenig M, et al. Among authors: kiuru a. Am J Hum Genet. 1989 Oct;45(4):498-506. Am J Hum Genet. 1989. PMID: 2491009 Free PMC article.
Diagnosis of Duchenne and Becker muscular dystrophies by polymerase chain reaction. A multicenter study.
Chamberlain JS, Chamberlain JR, Fenwick RG, Ward PA, Caskey CT, Dimnik LS, Bech-Hansen NT, Hoar DI, Richards S, Covone AE, Govanni R, Abbs S, Bentley DR, Bobrow M, Rysiecki G, Ray PN, Boileau C, Junien C, Boehm C, Venne VL, Fujmura FK, Spiga I, Ferrari M, Tedeschi S, Bakker E, Kneppers AL, van Ommen GJ, Jain K, Spector E, Crandall B, Kiuru A, Savontaus ML, Caskey CT, Chamberlain JS, Chamberlain JR, Rysiecki G. Chamberlain JS, et al. Among authors: kiuru a. JAMA. 1992 May 20;267(19):2609-15. doi: 10.1001/jama.1992.03480190051030. JAMA. 1992. PMID: 1573747 Clinical Trial.
Loss of SUFU function in familial multiple meningioma.
Aavikko M, Li SP, Saarinen S, Alhopuro P, Kaasinen E, Morgunova E, Li Y, Vesanen K, Smith MJ, Evans DG, Pöyhönen M, Kiuru A, Auvinen A, Aaltonen LA, Taipale J, Vahteristo P. Aavikko M, et al. Among authors: kiuru a. Am J Hum Genet. 2012 Sep 7;91(3):520-6. doi: 10.1016/j.ajhg.2012.07.015. Am J Hum Genet. 2012. PMID: 22958902 Free PMC article.
Comprehensive analysis of the role of DNA repair gene polymorphisms on risk of glioma.
Bethke L, Webb E, Murray A, Schoemaker M, Johansen C, Christensen HC, Muir K, McKinney P, Hepworth S, Dimitropoulou P, Lophatananon A, Feychting M, Lönn S, Ahlbom A, Malmer B, Henriksson R, Auvinen A, Kiuru A, Salminen T, Swerdlow A, Houlston R. Bethke L, et al. Among authors: kiuru a. Hum Mol Genet. 2008 Mar 15;17(6):800-5. doi: 10.1093/hmg/ddm351. Epub 2007 Nov 29. Hum Mol Genet. 2008. PMID: 18048407
p53 mutations in human head and neck cancer cell lines.
Kiuru A, Servomaa K, Grénman R, Pulkkinen J, Rytömaa T. Kiuru A, et al. Acta Otolaryngol Suppl. 1997;529:237-40. doi: 10.3109/00016489709124132. Acta Otolaryngol Suppl. 1997. PMID: 9288320
67 results