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Clinical and genetic heterogeneity in Meckel syndrome.
Paavola P, Salonen R, Baumer A, Schinzel A, Boyd PA, Gould S, Meusburger H, Tenconi R, Barnicoat A, Winter R, Peltonen L. Paavola P, et al. Among authors: salonen r. Hum Genet. 1997 Nov;101(1):88-92. doi: 10.1007/s004390050592. Hum Genet. 1997. PMID: 9385376
Tissue expression of nephrin in human and pig.
Kuusniemi AM, Kestilä M, Patrakka J, Lahdenkari AT, Ruotsalainen V, Holmberg C, Karikoski R, Salonen R, Tryggvason K, Jalanko H. Kuusniemi AM, et al. Among authors: salonen r. Pediatr Res. 2004 May;55(5):774-81. doi: 10.1203/01.PDR.0000117842.10241.2C. Epub 2004 Feb 5. Pediatr Res. 2004. PMID: 14764915
Mutant CHUK and severe fetal encasement malformation.
Lahtela J, Nousiainen HO, Stefanovic V, Tallila J, Viskari H, Karikoski R, Gentile M, Saloranta C, Varilo T, Salonen R, Kestilä M. Lahtela J, et al. Among authors: salonen r. N Engl J Med. 2010 Oct 21;363(17):1631-7. doi: 10.1056/NEJMoa0911698. N Engl J Med. 2010. PMID: 20961246 Free article.
316 results