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[Finnish disease heritage].
Kestilä M, Ikonen E, Lehesjoki AE. Kestilä M, et al. Duodecim. 2010;126(19):2311-20. Duodecim. 2010. PMID: 21086689 Review. Finnish.
The mutation spectrum in RECQL4 diseases.
Siitonen HA, Sotkasiira J, Biervliet M, Benmansour A, Capri Y, Cormier-Daire V, Crandall B, Hannula-Jouppi K, Hennekam R, Herzog D, Keymolen K, Lipsanen-Nyman M, Miny P, Plon SE, Riedl S, Sarkar A, Vargas FR, Verloes A, Wang LL, Kääriäinen H, Kestilä M. Siitonen HA, et al. Among authors: kestila m. Eur J Hum Genet. 2009 Feb;17(2):151-8. doi: 10.1038/ejhg.2008.154. Epub 2008 Aug 20. Eur J Hum Genet. 2009. PMID: 18716613 Free PMC article.
Assignment of the locus for PLO-SL, a frontal-lobe dementia with bone cysts, to 19q13.
Pekkarinen P, Hovatta I, Hakola P, Järvi O, Kestilä M, Lenkkeri U, Adolfsson R, Holmgren G, Nylander PO, Tranebjaerg L, Terwilliger JD, Lönnqvist J, Peltonen L. Pekkarinen P, et al. Among authors: kestila m. Am J Hum Genet. 1998 Feb;62(2):362-72. doi: 10.1086/301722. Am J Hum Genet. 1998. PMID: 9463329 Free PMC article.
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